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

BSP 1982-10-04

MONOJECT PLASTIC HUB SPINAL NEEDLE

Applicant Sherwood Medical Co.

K-Number K822630

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DSI 1982-10-04

SERIES 7000 BEDSIDE PATIENT MONITOR

Applicant Marquette Electronics, Inc.

K-Number K822718

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DPS 1982-10-04

ELECTROCARDIOGRAPH (74 DPS) #YM-102

Applicant Sanyo Electric, Inc.

K-Number K822768

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MBV 1982-10-04

TOTAL KNEE SYSTEM

Applicant Richard'S Medical Equip., Inc.

K-Number K822583

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DXY 1982-10-04

JAIN INSULATING BOOT MODEL 225B

Applicant Cook Pacemaker Corp.

K-Number K822652

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GWQ 1982-10-04

DEL MAR MODEL 5500 EEG SCANNER

Applicant Del Mar Avionics

K-Number K822700

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KCP 1982-10-04

EAR/ULCER SYRINGE

Applicant American Hospital Supply Corp.

K-Number K822754

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FPA 1982-09-30

BOSTON SOLUTION INFUSION SETS

Applicant The Boston Medical Group

K-Number K822406

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CGX 1982-09-30

FERMCOTEST CREATININE TEST REAGENT

Applicant Fermco Biochemics, Inc.

K-Number K822118

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KHQ 1982-09-30

T3 UPTAKE KITS

Applicant Pcl-Ria, Inc.

K-Number K822612

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FRN 1982-09-30

DELIVERY TUBE SET #2226

Applicant Delta Medical Industries

K-Number K822761

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DBF 1982-09-30

ANTISERA TO HUMAN FERRITIN

Applicant Kent Laboratories, Inc.

K-Number K822472

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