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

GZJ 1980-12-10

TRANSCUTANEOUS ELECTRIC NERVE STIMULATOR

Applicant General Medical Industries, Inc.

K-Number K802678

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IKY 1980-12-10

TETRA NATAL-MAT WATER FLOTATION MAT.

Applicant Tetra Group U.S.A., Inc.

K-Number K802833

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FQM 1980-12-10

ELASTIC OPEN WEAVE BANDAGE

Applicant Secol Co.

K-Number K802784

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FQM 1980-12-10

TUBULAR BANDAGE

Applicant Secol Co.

K-Number K802789

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KNK 1980-12-10

LANCER URIC ACID AUTO/STAT KIT

Applicant Sherwood Medical Co.

K-Number K802692

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KGX 1980-12-10

POROUS, BREATHING TAPE W/RELEASE LINER

Applicant Bioadhesive Systems, Inc.

K-Number K802752

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IYO 1980-12-10

DIOSCAN

Applicant Sonometrics Systems, Inc.

K-Number K802341

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IKY 1980-12-10

BEDDING PADS EGGCREATE PADS

Applicant Leemart Bedding Mfg. Co.

K-Number K802781

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LBI 1980-12-10

NEONATAL PHOTOTHERAPY UNIT

Applicant Ohio Medical Products

K-Number K802702

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ITG 1980-12-10

CELLONA

Applicant Secol Co.

K-Number K802792

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CDZ 1980-12-10

LIQUISOL TESTOSTERONE RADIOIMM. TEST KIT

Applicant Damon Corp.

K-Number K802661

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KGX 1980-12-10

ORTHOPEDIC PADDING

Applicant Secol Co.

K-Number K802795

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