Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k) Clearances

510(k) cleared devices tracked by MedTracker

HQH 1980-01-10

SCLERAL POWDER

Applicant Ocularists , Ltd.

K-Number K791923

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GEI 1980-01-10

MODEL III HANDSWITCH

Applicant Sara Dan, Inc.

K-Number K792600

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EAP 1980-01-09

DENTIX DENTAL X-RAY UNIT

Applicant Precise Optics

K-Number K792307

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HCC 1980-01-09

FEEDBACK EDR SYSTEM MODEL ME-1

Applicant Bio-Feedback Systems, Inc.

K-Number K792659

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ESD 1980-01-09

MODEL 339 TELECROS WIRELESS CROS

Applicant Telex Communications, Inc.

K-Number K792463

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IXO 1980-01-09

POST EXTRA SYSTOLIC POSTENTLATOR

Applicant Medrad, Inc.

K-Number K791959

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IWZ 1980-01-09

KODAK X-OMAT M20 PROCESSOR, MODEL 2

Applicant Eastman Kodak Company

K-Number K792434

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IYO 1980-01-09

ADR REAL-TIME SECTOR SCANNER

Applicant Adr Ultrasound

K-Number K792446

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CAP 1980-01-09

RESPIRATOR DISCONNECT ALARM CR 201

Applicant Intersect Medical Products, Inc.

K-Number K792516

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IWZ 1980-01-09

SR 301 MEDICAL X-RAY FILM

Applicant E.I. Dupont DE Nemours & Co., Inc.

K-Number K792317

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EAP 1980-01-09

RAFLEX 70

Applicant Mdt Corp., Inc.

K-Number K792437

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EFQ 1980-01-09

TRACHEOTOMY SPONGE, NON-ADHERENT BARRIER

Applicant American Medical Disposable, Inc.

K-Number K792617

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