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

IZO 1979-12-20

GIGANTOS 1012 MP

Applicant Siemens Corp.

K-Number K792393

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EXB 1979-12-20

STOMAHESIVE POWDER

Applicant E. R. Squibb & Sons, Inc.

K-Number K792382

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FPY 1979-12-20

TEMPORARY BURN SHEET WITH PERFORATED

Applicant American Medical Disposable, Inc.

K-Number K792432

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IZO 1979-12-20

POLYPHOS

Applicant Siemens Corp.

K-Number K792392

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FPA 1979-12-20

CONTINU-FLO ADMIN. SET CODE 2C/200

Applicant Travenol Laboratories, S.A.

K-Number K792538

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FMR 1979-12-20

SKIL-CARE TURN AND HOLD PAD

Applicant Skil-Care Corp.

K-Number K792318

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FNJ 1979-12-20

THE VERSA-BED

Applicant First & Ten, Inc.

K-Number K792298

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GEN 1979-12-20

CATHETERIZATION FORCEP

Applicant C. Intl.

K-Number K792494

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EOQ 1979-12-19

PENTEX BRONCHOFIBERSCOPE MODEL FB-17A

Applicant Pentax Precision Instrument Corp.

K-Number K792267

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JEC 1979-12-19

MINI-H-FIXATION

Applicant Geny Medical, Inc.

K-Number K792561

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DWS 1979-12-19

CASTROVIEJO VASCULAR SCISSORS

Applicant Edward Weck, Inc.

K-Number K792576

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JSJ 1979-12-19

KF STREPTOCOCCUS AGAR

Applicant Isle Media and Sterile Products, Inc.

K-Number K792287

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