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

EXB 1980-08-27

SUR-FIT SYSTEM PRE-OPERATION SET

Applicant E. R. Squibb & Sons, Inc.

K-Number K801702

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DJA 1980-08-27

GAS-CHROMATOGRAPHIC PACKING

Applicant Supelco, Inc.

K-Number K801833

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FNG 1980-08-27

DRUALIFT 500

Applicant Independent Transfer Equipment Co.

K-Number K801933

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BZQ 1980-08-27

RESPONDER II

Applicant Clinical Microsystems Intl.

K-Number K801894

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FRG 1980-08-22

AMPCO DRESSING CHANGE TRAYS

Applicant Associated Medical Products Co.

K-Number K801333

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DZA 1980-08-20

DRILL, DENTAL

Applicant Aesculap Instruments Corp.

K-Number K801887

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GCY 1980-08-20

JACKSON-PRATT LARGE VOL. CLOSED WOUND

Applicant American Heyer Schulte

K-Number K801766

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IPF 1980-08-20

INTELECT

Applicant Chattanooga Group, Inc.

K-Number K801790

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IYN 1980-08-20

DOPPLER ULTRASONIC STETHOSCOPE

Applicant Mountain Medical Equipment, Inc.

K-Number K801512

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GDY 1980-08-20

CONTAIN X-RAY DETECTABLE LAP SPONGE

Applicant The Buckeye Cellulose Corp.

K-Number K801768

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FOZ 1980-08-20

L-CATH INTRAVENOUS PLACEMENT UNIT

Applicant Luther Medical Products, Inc.

K-Number K801575

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DXO 1980-08-20

MMI/GAELTEC CATHETER TIP TRANSDUC

Applicant Medical Measurements, Inc.

K-Number K801756

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