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

JOK 1977-04-29

SHEAR, PLASTIC HANDLE UTILITY S-475-7

Applicant Acme United Corp.

K-Number K770481

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ERA 1977-04-29

OTOSCOPE/ILLUMINATOR, MODEL #21100

Applicant Welch Allyn, Inc.

K-Number K770769

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FMC 1977-04-29

LACERATION KIT

Applicant American Hospital Supply Corp.

K-Number K770479

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KME 1977-04-29

SHEET KIT, STRETCHER, DISPOSABLE

Applicant American Hospital Supply Corp.

K-Number K770486

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CDH 1977-04-29

URIC ACID PROCEDURE, TEKPOINT DIRECT

Applicant Icn Pharmaceuticals, Inc.

K-Number K770459

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FOG 1977-04-28

DUODENOSCOPE, MOLEL TX-6

Applicant American Cystocope Makers, Inc.

K-Number K770754

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DFK 1977-04-28

FLOR. CONJUG. HUMAN FAB FRAGMENT

Applicant Kent Laboratories, Inc.

K-Number K770670

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KOC 1977-04-28

GAMBRO VENOUS BLOOD LINE

Applicant Gambro, Inc.

K-Number K770691

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ITG 1977-04-28

CUTTER CAST 7

Applicant Cutter Laboratories, Inc.

K-Number K770742

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DEW 1977-04-28

RHODAMINE-CONJUGATED ANTISERUM

Applicant Kent Laboratories, Inc.

K-Number K770669

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GEI 1977-04-28

ELECTROSURGICAL PATIENT GROUNDING PAD

Applicant C.R. Bard, Inc.

K-Number K770646

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N/A 1977-04-28

INTRAOCULAR LENS

Applicant Milton Roy Co. Analytical

K-Number K770728

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