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Adtemp™ 416-50

by American Diagnostic Corporation

Adtemp™ 416-50 is a Class II device made by American Diagnostic Corporation, cleared under FDA 510(k) K202009 on 22 Mar 2021 (1 earlier submission) and listed in FDA GUDID since 27 Apr 2018 (UDI-DI 00634782053673), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK202009 Date22 Mar 2021DecidedStatusActive
United StatesGUDID listing Number00634782053673 UDI-DI Date27 Apr 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • FDA 510(k) K202009 decided 22 Mar 2021 Active· +1 more in the status table
  • FDA GUDID UDI-DI 00634782053673 listed 27 Apr 2018 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K940686
  2. Listed FDA GUDID 00634782053673
  3. Cleared FDA 510(k) K202009

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Adtemp™
Generic name
Electronic thermometer probe cover
Model / Ref / Catalog
416-50
Primary DI / UDI-DI
00634782053673
510(k) Number
FDA product code
FLL
GMDN term
Electronic thermometer probe cover
Device class
Class II
Regulation number
880.2910
GUDID distribution status
In Commercial Distribution

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Properties

  • Over-the-counter
  • Lot / batch number
Other properties (13, all answered No)