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Episcope, Model 47300

by Welch Allyn, Inc.

510(k) K920103

Episcope, Model 47300 is a Class I device made by Welch Allyn, Inc., cleared under FDA 510(k) K920103 on 28 Apr 1992, 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 NumberK920103 Date28 Apr 1992ClearedStatusActive

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  • Withdrawn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
KZF
Device class
Class I
Regulation
21 CFR Part 880.6320
Advisory committee
General Hospital
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code KZF (Device, Medical Examination, Ac Powered).

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