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

FPA 1981-06-12

IV SETS

Applicant Critikon Company, LLC

K-Number K811107

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KMF 1981-06-12

HYDRON WOUND DRESSING KIT

Applicant National Patent Development Corp.

K-Number K811446

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JTW 1981-06-12

GC TTANSPORT SYSTEM

Applicant Biolog, Inc.

K-Number K811284

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JTY 1981-06-12

GC CULTURE MEDIUM

Applicant Biolog, Inc.

K-Number K811281

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HGX 1981-06-12

AXICARE BREAST PUMP MODEL

Applicant Neonatal Corp.

K-Number K811403

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DHX 1981-06-12

CEA DESALTING DOLUMN SEPHADEX R

Applicant Immuno-Diagnostic Laboratories

K-Number K811394

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FPA 1981-06-12

AUTO-SYRINGE MICRO VOLUME EXTENSION SET

Applicant Baxter Healthcare Corp

K-Number K811463

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DXG 1981-06-12

BAIM CORONARY SINUS FLOW ANALYZER

Applicant Electro-Catheter Corp.

K-Number K811414

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ILD 1981-06-12

DRESSING ADAPTORS

Applicant Fred Sammons, Inc.

K-Number K811492

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JJY 1981-06-12

AMITRIPTYLINE/NORTRIPTYLINE/LITHIUM

Applicant Ortho Diagnostic Systems, Inc.

K-Number K811466

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DCN 1981-06-12

BI-CRP LATEX TEST

Applicant Biologics Intl., Inc.

K-Number K811374

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JTY 1981-06-12

SELECTIVE GC CULTURE MEDIUM

Applicant Biolog, Inc.

K-Number K811282

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