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

FJI 1977-01-12

ARTIFICIAL KIDNEY, C-DAK CORDIS DOW

Applicant Cordis Corp.

K-Number K761007

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KKX 1977-01-12

BARRIER IMPERVIOUS BACK TABLE COVER

Applicant Surgikos, Inc.

K-Number K761204

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ILQ 1977-01-12

ALARM INTERCOM DOOR LOCK

Applicant Possum, Inc.

K-Number K770031

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JOZ 1977-01-12

AGGRECETIN

Applicant Bio/Data Corp.

K-Number K760893

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KRA 1977-01-12

FLUSHFLO-MODEL CC1-6

Applicant Bentley Laboratories, Inc.

K-Number K761273

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FHS 1977-01-10

COIL DIALYZER MODEL ALT 140

Applicant Bentley Laboratories, Inc.

K-Number K761358

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ION 1977-01-10

FLEXION-BRAKING KNEE-SHIN ASSEMBLY

Applicant Hosmer Dorrance Corp.

K-Number K761314

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GJE 1977-01-10

SODIUM CITRATE

Applicant Bio/Data Corp.

K-Number K761177

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GKT 1977-01-10

BLOOD CELL PROCESSOR MODEL 2 IBM 2991

Applicant Intl. Business Machines

K-Number K760856

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JCE 1977-01-10

BARBITAL SALINE BUFFER

Applicant Bio/Data Corp.

K-Number K761170

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KNX 1977-01-10

8 LATEX EXTENSION TUBE WITH CONNECTOR

Applicant Intermed, Inc.

K-Number K761360

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JRR 1977-01-10

AQUAMATIC K-MODULE MODEL K-10

Applicant Gorman Rupp Industries

K-Number K761337

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