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

CFJ 1983-01-09

FLOW-PAC LDH REAGENT SET

Applicant Amresco, Inc.

K-Number K823721

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CDQ 1983-01-09

BUN-UN CENTRIFICHUM 500, #65080/81

Applicant Emd Chemicals, Inc.

K-Number K823300

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EMI 1983-01-09

DISC NEEDLE SET #TX-8220

Applicant Today'S Machining & Design, Inc.

K-Number K823676

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JQP 1983-01-09

API MDS*

Applicant Analytical Products, Inc.

K-Number K823785

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KOD 1983-01-09

CATHETER HOLDER

Applicant Danek Medical, Inc.

K-Number K823818

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DYH 1983-01-09

ORTHODAPTIC* BONDING ADHESIVE

Applicant Johnson & Johnson Professionals, Inc.

K-Number K823851

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GEF 1983-01-09

3M FRASCIA STAPLING SYSTEM

Applicant 3M Company

K-Number K823888

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GDY 1983-01-09

NO-GAUZE LAPAROTOMY SPONGE

Applicant Surgilite Intl., Inc.

K-Number K823671

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LJG 1983-01-09

Q-CHECK REAGENT STANDARDS

Applicant Lab Ability, Inc.

K-Number K830134

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FRG 1983-01-09

EAGLE STERISET

Applicant American Sterilizer Co.

K-Number K823902

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GEI 1983-01-09

MODEL SSE4 ELECTROSURGICAL GENERATOR

Applicant Valleylab, Inc.

K-Number K823924

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DTB 1983-01-08

ELECTRODE LEAD OF SILICONE ELASTOMETER

Applicant Telectronics, Inc.

K-Number K823452

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