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

KBC 1981-03-20

AUTO SUTURE GAS POWERED DISP. LDS STAPL

Applicant United States Surgical, A Division of Tyco Healthc

K-Number K810188

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GMD 1981-03-20

YA-CRYPTO ANTIBODY TUBE AGGLUTINATION

Applicant Immuno-Mycologics, Inc.

K-Number K810510

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LYC 1981-03-20

HYDROXYLAPATITE ALVEOLAR RIDGE MAIN

Applicant Carbomedics, Inc.

K-Number K810382

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KRG 1981-03-20

CORDIS PACEMAKER PROGRAMMERS 255A & 256A

Applicant Cordis Corp.

K-Number K810552

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HAX 1981-03-20

TRIPPI-WELLS DUAL PURPOSE UNIVERSAL TONG

Applicant Ace Orthopedic Manufacturing Co.

K-Number K810193

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KOB 1981-03-20

VANCE PERCUTANEOUS MALECOT NEPHROSTOMY

Applicant Vance Products, Inc.

K-Number K810368

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DTB 1981-03-20

TYPE YR ENDOCARDIAL LEAD

Applicant Biotronik Sales, Inc.

K-Number K810492

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JSK 1981-03-20

PACT SUPPLEMENT

Applicant Bd Becton Dickinson Vacutainer Systems Preanalytic

K-Number K810591

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KBC 1981-03-20

AUTO SUTURE PSS SKIN STAPLING INSTRUMENT

Applicant United States Surgical, A Division of Tyco Healthc

K-Number K810187

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DTB 1981-03-20

TYPE N ENDOCARDIAL LEAD

Applicant Biotronik Sales, Inc.

K-Number K810493

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FJG 1981-03-20

CYBER 120 HEMODIALYZER

Applicant Cyberex Corp.

K-Number K802478

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N/A 1981-03-20

TRANSCUTANEOUS ELECT. NERVE STIMULATOR

Applicant Medical Research Laboratories, Inc.

K-Number K803247

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