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AcuityPDR

by Radmedix, LLC

510(k) K200726

AcuityPDR is a medical device (FDA Class II; FDA product code IZL, System, X-Ray, Mobile) made by Radmedix, LLC, cleared under FDA 510(k) K200726 on 13 Apr 2020, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK200726 Date13 Apr 2020ClearedStatusActive

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
IZL
Device class
Class II
Regulation
21 CFR Part 892.1720
Advisory committee
Radiology
FDA decision
SESE Substantially Equivalent

Devices cleared under K200726

26 devices · FDA GUDID

Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.

Devices cleared under K200726
UDI-DISize and differences
AcuityPDR Standard
Radmedix, LLC
Standard00810035220119
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220331
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220164
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220287
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220249
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220201
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220218
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220256
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220232
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220171
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220270
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220140
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220362
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220188
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220294
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220126
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220355
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220195
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220157
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220225
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220263
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220348
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220133
Prescription: no
On the market
AcuityPDR Standard
Radmedix, LLC
Standard00810035220300
Prescription: no
On the market
Radmedix AcuityPDR 1
Radmedix, LLC
100810035220430
Prescription: no
On the market
Radmedix AcuityPDR+ 1
Radmedix, LLC
100810035220461
Prescription: yes
On the market

Similar devices

Other devices filed under FDA product code IZL (System, X-Ray, Mobile).

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