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

KHW 1981-02-25

CORDIA A

Applicant Cordis Corp.

K-Number K810046

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DXG 1981-02-25

PATIENT MONITOR MODEL CM130, 140

Applicant Honeywell, Inc.

K-Number K810177

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N/A 1981-02-25

URISTOP

Applicant The Sora Co.

K-Number K803109

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IZI 1981-02-25

PRO-TOP-ANGIO SHIFT TABLE TOP EXTENSION

Applicant Philips Medical Systems (Cleveland), Inc.

K-Number K810183

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DXJ 1981-02-25

SLAVE MONITORS DC109 & VS109

Applicant Honeywell, Inc.

K-Number K810168

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KHS 1981-02-23

BICARBONATE TEST

Applicant Boehringer Mannheim Corp.

K-Number K810356

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ISA 1981-02-23

PERCUSS-O-FLEX FOOT & HAND MASSAGER

Applicant Modern Reflexology, Inc.

K-Number K810354

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DXY 1981-02-23

UNIFOCAL 3

Applicant American Pacemaker Corp.

K-Number K810121

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JDB 1981-02-23

TRIAXIAL

Applicant Johnson & Johnson Professionals, Inc.

K-Number K802348

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CKA 1981-02-23

ALT (UV) TEST

Applicant Boehringer Mannheim Corp.

K-Number K810355

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LZN 1981-02-23

HARRIS CEMENT RESTRICTOR

Applicant Cintor Orthopaedic Div.

K-Number K810353

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CBP 1981-02-23

CM 3

Applicant Instrumentation Industries, Inc.

K-Number K810348

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