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

KKX 1982-01-22

BOUNDARY SINGLE-USE DRAPES

Applicant The Buckeye Cellulose Corp.

K-Number K813450

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ETD 1982-01-22

TEKNA MED MYRINGOTOMY DISPOS-OTO KIT

Applicant Humboldt Products

K-Number K813616

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GCX 1982-01-22

DS-7 CLOSED WOUND SUCTION DRAIN SYSTEM

Applicant Cox-Uphuff Intl.

K-Number K813394

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DXQ 1982-01-22

CONPHAR PALM ANEROID SPHYGMOMANOMETER

Applicant Conphar, Inc.

K-Number K813302

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HMX 1982-01-22

OMS INFUSION CANNULA ASSEMBLE

Applicant Optical Micro Systems, Inc.

K-Number K813481

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DPS 1982-01-22

CARDIOSTRESS

Applicant Instruments For Cardiac Research

K-Number K820011

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EFT 1982-01-22

SPRYCE, DENTURE CLEANSER

Applicant Richardson-Vicks, Inc.

K-Number K820020

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JDI 1982-01-22

AUFRANC-TURNER TYPE ACETABULAR COMPON

Applicant Intermedics Orthopedics

K-Number K813600

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JIX 1982-01-22

SODIUM & POTASSIUM PRODUCTS

Applicant Alko Diagnostic Corp.

K-Number K813127

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HQF 1982-01-22

BRITT KRYPTON LASERS 150K & 152K

Applicant Britt Corp., Inc.

K-Number K813492

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EBF 1982-01-22

ZEON COMPOSITE RESIN SYSTEM

Applicant National Patent Development Corp.

K-Number K820006

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DXY 1982-01-22

SIEMENS-ELEMA PULSE GENERATOR 659

Applicant Siemens Elema AB

K-Number K813576

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