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

JQW 1977-02-14

ANALYTIX AUTO SAMPLE PREP. STA. 1600

Applicant G.D. Searle and Co.

K-Number K770210

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DRT 1977-02-14

DIGITAL HEART RATE METER

Applicant Burdick Corp.

K-Number K770239

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HNL 1977-02-14

NASO-LACRIMAL DUCT INSERT

Applicant Concept, Inc.

K-Number K770194

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KXN 1977-02-14

ABDOMINAL FETAL ECG MODULE

Applicant Mennen Greatbatch Electonics

K-Number K770245

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CDX 1977-02-14

NEONATAL T4 RIA KIT

Applicant Diagnostic Products Corp.

K-Number K770241

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DRR 1977-02-14

ELGILOY STYLET

Applicant Cardiac Pacemakers, Inc.

K-Number K770243

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JJJ 1977-02-14

GAMMA 4000 SCINTILLATION COUNTER

Applicant Beckman Instruments, Inc.

K-Number K770088

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CGA 1977-02-11

REFLOMAT/REFLOTEST SYSTEM

Applicant Boehringer Mannheim Corp.

K-Number K761148

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JIX 1977-02-11

SMA REFERENCE SERUM 3

Applicant Technicon Instruments Corp.

K-Number K770142

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CGX 1977-02-11

AUTO CREATININE REAGENT (ABBOTT SYSTEM)

Applicant Harleco

K-Number K761279

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BTO 1977-02-09

SHILEY PEDIATRIC MURPHY ENDOTRACH. TUBE

Applicant Shiley, Inc.

K-Number K770218

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FSD 1977-02-09

MATERNITY SUPPORTER

Applicant R.G. Moore

K-Number K770162

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