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

KDJ 1978-01-24

PERITONEAL DIALYSIS ADMIN. SET

Applicant Physio-Control Corp.

K-Number K780082

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DDX 1978-01-24

LAS-R HUMAN PLASMINOGEN TEST

Applicant Hyland Therapeutic Div., Travenol Laboratories

K-Number K772085

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KKX 1978-01-24

TOWEL, DRAPE, BOUNDARY

Applicant Procter & Gamble Mfg. Co.

K-Number K780036

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JZH 1978-01-24

LAS-R HUMAN C3 PROACTIVATOR TEST

Applicant Hyland Therapeutic Div., Travenol Laboratories

K-Number K772084

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GXY 1978-01-24

ELECTRODE CAP

Applicant Electro-Cap Intl., Inc.

K-Number K780045

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KDJ 1978-01-24

FILTER, PERITONEAL DIALY. ADMIN. SET

Applicant Millipore Corp.

K-Number K772236

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KCW 1978-01-24

EPILATOR, ELECTRONIC MODEL SE-2

Applicant R. A. Fischer Co. Corp.

K-Number K780076

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DQD 1978-01-24

STETHOSCOPE, ELECTRONIC

Applicant Affiliated Mailorder Co. Sales, Inc.

K-Number K772173

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DRC 1978-01-24

NEEDLES USED IN ANGIOGRAPHIC PROCED.

Applicant Argon Medical Corp.

K-Number K772369

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CEX 1978-01-24

LDH ISOENZYME COLUMN REAGENT SET

Applicant Worthington Biochemical Corp.

K-Number K772356

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DXY 1978-01-24

PULSE GENERATORS, MODELS 5972/5973

Applicant Medtronic Vascular

K-Number K780061

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CGC 1978-01-20

GASTRIN RIA MODULE

Applicant Inter Science Institute

K-Number K771953

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