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

CZQ 1980-10-23

ANTISERA TO HUMAN FREE LAMBDA LIGHT CH.

Applicant Kallestad Laboratories, Inc.

K-Number K802284

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FOS 1980-10-23

UMBILI-CATH CATHETER

Applicant Int'L Corp.

K-Number K802414

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KNS 1980-10-23

PAPILLOTOME PRODUCT

Applicant Mill-Rose Laboratory

K-Number K802444

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FJS 1980-10-23

TENCKHOFF CATHETER

Applicant Sil-Med Corp.

K-Number K801818

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JSG 1980-10-23

ANAEROBE BLOOD AGAR

Applicant Granite Diagnostics, Inc.

K-Number K802397

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FRG 1980-10-23

PROPPER SHARPGUARD & TRAYPAD STERIL. AID

Applicant Propper Mfg. Co., Inc.

K-Number K802428

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HGX 1980-10-23

MEDELA ELECTRIC BREAST PUMP

Applicant Medela, Inc.

K-Number K801862

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KGZ 1980-10-23

ARGLE LATEX PENROSE TUBING

Applicant Sherwood Medical Co.

K-Number K802286

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DWI 1980-10-23

TEMP STERNUM SAW

Applicant Temp Medical Products, Inc.

K-Number K801914

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IZJ 1980-10-23

105MM SPOT FILM CAMERA

Applicant Instrumentation Camera, Inc.

K-Number K802132

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KNT 1980-10-23

VIVONEX JEJUNOSTOMY KIT

Applicant Norwich Eaton Pharmaceuticals, Inc.

K-Number K802300

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BSR 1980-10-23

SALEM/RESCE INTUBATION GUIDE

Applicant Scientific Sales Intl., Inc.

K-Number K802416

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Page 13330 of 14146

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