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FDA 510(k)

REPLACEMENT BATTERIES/WELCH ALLYN #72200 POWER HANDLE

K-Number: K942244 · 1994-06-24

ApplicantNational Custom Ent., Inc.
Decision Date1994-06-24
Product CodeERA
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

REPLACEMENT BATTERIES/WELCH ALLYN #72200 POWER HANDLE is the device name listed in this FDA 510(k) record. The listed applicant is National Custom Ent., Inc.. It received FDA 510(k) clearance on 1994-06-24 under 510(k) number K942244. The device is classified under product code ERA. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPLACEMENT BATTERIES/WELCH ALLYN #72200 POWER HANDLE?

REPLACEMENT BATTERIES/WELCH ALLYN #72200 POWER HANDLE is a medical device that received FDA 510(k) clearance on 1994-06-24. The listed applicant is National Custom Ent., Inc.. The 510(k) number is K942244.

When did REPLACEMENT BATTERIES/WELCH ALLYN #72200 POWER HANDLE receive FDA 510(k) clearance?

REPLACEMENT BATTERIES/WELCH ALLYN #72200 POWER HANDLE received FDA 510(k) clearance on 1994-06-24, under 510(k) number K942244.

Who is the listed applicant for REPLACEMENT BATTERIES/WELCH ALLYN #72200 POWER HANDLE?

The FDA 510(k) record lists National Custom Ent., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REPLACEMENT BATTERIES/WELCH ALLYN #72200 POWER HANDLE?

The FDA product code for REPLACEMENT BATTERIES/WELCH ALLYN #72200 POWER HANDLE is ERA.

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Other records listing National Custom Ent., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K012263MARQUETTE EAGLE MONITOR MODEL 4000, MODEL N3024K012264MARQUETTE MAC8, MAC PERSONAL, MAC STRESS, MODEL N3043IWCK012266SHERWOOD 224, 324 FEEDING PUMP & K524 INTRI-FLUSH, MODEL N7213IWC2K012262BAXTER AS40A, AS41 SYRINGE PUMP, MODEL N61WCK012259MEDFUSION 2001 & 2010, MODEL N7215IWCK012229SCALE-TRONIX 48, 2001, 2009,2700,3003,4004, 4800, 5005,5700,6005,6500,6700,6006C & 20009, MODEL N661WC

View all 12 devices →

Related Devices (Code: ERA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K123821AIO HD OTOSCOPEBlue FocusK121326LANTOS 3D EAR SCANNERLantos TechnologiesK110326OSRAM ITOSOsram Sylvania, Inc.K945264OPTUS OTOSCOPESOptus, Inc.K955043WELCH ALLYN BI-OTOSCOPEWelch Allyn, Inc.K952578WELCH ALLY OTOSCOPEWelch Allyn, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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