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

FLE 1977-05-20

STERILIZER, SERIES 3000, MODIFICATION TO

Applicant Castle Co.

K-Number K770682

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GQG 1977-05-20

RESP. SYNCYTIAL-FA LABELLED PRESERUM

Applicant Flow Laboratories, Inc.

K-Number K770808

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HHD 1977-05-20

MAXI-PADS, STAYFREE

Applicant Personal Products Co.

K-Number K770778

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GOL 1977-05-20

MEASLES-FA LABELED PRESERUM (8-441 RNF)

Applicant Flow Laboratories, Inc.

K-Number K770809

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N/A 1977-05-18

RECORDING UNIT, MODEL 1445

Applicant Scole Engineering Co.

K-Number K770829

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EWO 1977-05-18

AUDIOMETRIC TESTING SYS., SERIES 500

Applicant Automated Testing Services, Ltd.

K-Number K770823

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ILH 1977-05-18

SPLINTS, FINGER/TOE

Applicant Depuy, Inc.

K-Number K770786

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FOZ 1977-05-10

CANNULA, INTRAVENOUS, TEFLON

Applicant Sherwood Medical Industries

K-Number K770510

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KNX 1977-05-10

BAG, URINARY, DRAINAGE, 2D9013

Applicant Travenol Laboratories, S.A.

K-Number K770762

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IYX 1977-05-10

PORTA CAMERA IIC

Applicant General Electric Co.

K-Number K770753

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EGY 1977-05-10

FILM PROCESSOR, AUTOMATIC

Applicant General Electric Co.

K-Number K770783

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FJI 1977-05-10

DIALYZER, FIBER, HOLLOW

Applicant Travenol Laboratories, S.A.

K-Number K770734

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