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Rnk Electronic Stethoscope

by Rnk Products, Inc.

510(k) K072026

Rnk Electronic Stethoscope is a Class II device made by Rnk Products, Inc., cleared under FDA 510(k) K072026 on 26 Oct 2007, 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 NumberK072026 Date26 Oct 2007ClearedStatusActive

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  • Withdrawn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
DQD
Device class
Class II
Regulation
21 CFR Part 870.1875
Advisory committee
Cardiovascular
FDA decision
SESE Substantially Equivalent

Related clearances

Clearances this device's FDA summary refers to, and clearances whose summaries refer to it: a citation, not a claim of equivalence.

Cited by

Source: 510k-lineage (choiben314), CC BY 4.0

Devices cleared under K072026

1 device · 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 K072026
UDI-DISize and differences
RNK Products PCP
Rnk Products, Inc.
PCP00677986002009 —On the market

Similar devices

Other devices filed under FDA product code DQD (Stethoscope, Electronic).

Other devices from Rnk Products, Inc.

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