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

DXG 1980-10-10

MLC-4200 CARDIAC OUTPUT COMPUTER

Applicant Nihon Kohden America, Inc.

K-Number K802305

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LFI 1980-10-10

7 TRICYCLIC ANTIDE PRESSANTS

Applicant Technicon Instruments Corp.

K-Number K802245

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KXT 1980-10-10

OREIA-Q-DIG

Applicant Organon, Inc.

K-Number K802358

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GKL 1980-10-10

ORTHO SPECTRUM

Applicant Ortho Instruments

K-Number K802094

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CDT 1980-10-10

DELTA TEST TRIGLYCERIDES

Applicant Bd Becton Dickinson Vacutainer Systems Preanalytic

K-Number K802136

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JTN 1980-10-10

MINOCYCLINE 30 MCG. SENSITIVITY DISCS

Applicant Difco Laboratories, Inc.

K-Number K802178

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DTZ 1980-10-10

DISP. TOUGY-BORST TYPE ADAPTOR W/PORT

Applicant Stanco Medical, Inc.

K-Number K802328

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CGX 1980-10-10

REAGENTS SERUM CREATINE USING TECHICON

Applicant Panmed, Inc.

K-Number K802156

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ILJ 1980-10-10

WHIRLPOOL BATHING UNIT-#2001

Applicant Aqua Care Corp.

K-Number K802335

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HHL 1980-10-10

KOTEX LIGHTDAYS DEODORANT PANTILINERS

Applicant Kimberly-Clark Corp.

K-Number K802277

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GHH 1980-10-10

FIBRIN(OGEN) DEGRADATION PRODUCTS(FDP)

Applicant American Hospital Supply Corp.

K-Number K801841

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FPX 1980-10-10

OP-SITE SKIN CLOSURE SUTURE ADHESIVE

Applicant Acme United Corp.

K-Number K801884

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