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

FRN 1977-07-11

PUMP, INFUSION, DYNATECH/HANDLEY

Applicant Dynatech Medical Products

K-Number K770730

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HTD 1977-07-11

LOWMAN BONE FORCEP

Applicant Edward Weck, Inc.

K-Number K771192

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GCY 1977-07-11

VYGON RED-O-PACK

Applicant Coastal Bend Medical Products, Inc.

K-Number K771015

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JJX 1977-07-11

SHAVE PREP SET

Applicant Lukens Corp.

K-Number K770795

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GHO 1977-07-11

EMATOLOGY DILUENT RESERVOIR CLOSURE

Applicant Bd Becton Dickinson Vacutainer Systems Preanalytic

K-Number K770980

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GKL 1977-07-11

COUNTER 700 & HC-700 HEMO 0 REF.

Applicant Hycel, Inc.

K-Number K771107

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CIX 1977-07-11

A-GENT ALBUMIN

Applicant Abbott Laboratories

K-Number K770822

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GLE 1977-07-11

PLATELET AGITATOR

Applicant Helmer Labs, Inc.

K-Number K770830

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CEM 1977-07-11

CENTRIA SEPARATION COLUMNS TYPE A

Applicant Clinical Diagnostics, Inc.

K-Number K771118

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CHH 1977-07-11

REAGENTS

Applicant Chemetrics Corp.

K-Number K770780

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HQP 1977-07-11

HOT TEMP CAUTERY

Applicant Edward Weck, Inc.

K-Number K771189

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N/A 1977-07-11

SPECTROPHOTOMETERS,34,35,36,3600

Applicant Beckman Instruments, Inc.

K-Number K770825

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