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

EPY 1978-01-17

THIN-BLADED NASAL SPECULUM

Applicant Edward Weck, Inc.

K-Number K772385

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IQI 1978-01-17

BRACE, TENNIS ELBOW

Applicant Bd Becton Dickinson Vacutainer Systems Preanalytic

K-Number K780053

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JYO 1978-01-17

MYRINGOTOMY KNIFE

Applicant Edward Weck, Inc.

K-Number K772384

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EPY 1978-01-17

FARRIOR OVAL SPECULUM

Applicant Edward Weck, Inc.

K-Number K772380

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KAE 1978-01-17

ALLIGATOR CUP FORCEPS

Applicant Edward Weck, Inc.

K-Number K772396

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GZB 1978-01-17

EPIDURAL LEAD - MODEL 3481

Applicant Medtronic Vascular

K-Number K780001

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JYL 1978-01-17

DAY EAR HOOK

Applicant Edward Weck, Inc.

K-Number K772390

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DXY 1978-01-17

PULSE GENERATORS

Applicant Medtronic Vascular

K-Number K772357

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KAD 1978-01-17

BOIES NASAL FRACTURE ELEVATOR

Applicant Edward Weck, Inc.

K-Number K772391

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IMG 1978-01-13

MUSCLE STIMULATOR

Applicant Rich-Mar Corp.

K-Number K772287

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JAD 1978-01-13

EMI THERAPY SIMULATOR

Applicant Emi Therapy Systems, Inc.

K-Number K771817

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CDX 1978-01-12

T4 RIA KIT

Applicant Bd Becton Dickinson Vacutainer Systems Preanalytic

K-Number K772330

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