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

KZD 1982-08-27

AUTOCUFF (PHOTOS ENCLOSED WITH 510K

Applicant Partamed, Inc.

K-Number K822286

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GBS 1982-08-27

ARGYLE MEDIASTINAL DRAIN

Applicant Sherwood Medical Co.

K-Number K822318

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N/A 1982-08-27

MODEL 57000 NASO-CONJUNCTIVA ISOL. MASK

Applicant Welch Allyn, Inc.

K-Number K822125

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JQW 1982-08-27

CAVRO IQ-190 SAMPLE PROCESSOR

Applicant Cavro Scientific Instruments, Inc.

K-Number K822208

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KOA 1982-08-27

ST. MARK'S RECTAL BIOPSY FORCEPS

Applicant Keymed, Inc.

K-Number K822401

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KOC 1982-08-27

TS-000 ARTERIOVENOUS BLOOD TUBING SET

Applicant Extracorporeal Medical Specialities, Inc.

K-Number K822283

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HMN 1982-08-25

MYOCUR BLADE PAC

Applicant Myocure, Inc.

K-Number K822392

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GWJ 1982-08-25

AUDIOMETERS (VARIOUS MODELS)

Applicant Kelleher Corp.

K-Number K822177

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HHK 1982-08-25

U.V.A.C. HANDLER SET

Applicant American Hospital Supply Corp.

K-Number K822382

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KAK 1982-08-25

ROSEN'S STAPES NEEDLE EXPLORER

Applicant Kelleher Corp.

K-Number K822277

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KLR 1982-08-25

LIDOCAINE FLUORESCENT IMMUNOASSAY

Applicant American Diagnostic Corp.

K-Number K822347

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EPF 1982-08-25

STIMRITE

Applicant Biotone International, Inc.

K-Number K821691

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