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

DZN 1980-07-28

COREFORM MOLDS

Applicant Sybron Corp.

K-Number K801530

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DWF 1980-07-28

PRUITT VASCULAR SHUNT

Applicant Ideas For Medicine, Inc.

K-Number K801359

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ITG 1980-07-28

IPOCON 7

Applicant Ipos Luneburg

K-Number K800749

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KNT 1980-07-28

NASO-GARD NASOGASTRIC TUBE HOLDER

Applicant Howmedica Corp.

K-Number K801511

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FYB 1980-07-28

SHIELD DISP. PATIENTS PONCHO GOWNS

Applicant American Convertors Div., American Pharmaseal

K-Number K801570

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N/A 1980-07-28

RETREAT

Applicant Omnitronics Research Corp.

K-Number K801606

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HNR 1980-07-28

GASKIN FRAGMENT FORCEPS(MFG. NON-STERILE

Applicant Edward Weck, Inc.

K-Number K801465

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JAK 1980-07-28

SYNERVIEW MODEL 6545

Applicant Philips Medical Systems (Cleveland), Inc.

K-Number K801407

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DTS 1980-07-28

OHIO DISPOSABLE CLEAR SUCTION INSTRUMENT

Applicant Ohio Medical Products

K-Number K801641

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JTN 1980-07-28

CINOXACIN 100 MCG. SENSITIVITY DISCS

Applicant Difco Laboratories, Inc.

K-Number K801473

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DXF 1980-07-28

BLADE SEPTOSTOMY CATHETER

Applicant Cook, Inc.

K-Number K801031

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KDP 1980-07-28

OHIO FREE FLOW VACUUM REGULATOR

Applicant Ohio Medical Products

K-Number K801169

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