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

DIF 1978-12-07

SERUM, CONTROL, DRUGS, ANTIARRYTHMIC

Applicant Vitek Systems, Inc.

K-Number K780960

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KPO 1978-12-07

HEMODIALYSIS CONCENTRATE, SODIU

Applicant Renal Systems, Inc.

K-Number K781967

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KME 1978-12-07

ROSEALAE

Applicant Asmb

K-Number K782001

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HHM 1978-12-07

UTERINE SOUND, BURNETT DISPOSABLE

Applicant C.R. Bard, Inc.

K-Number K781766

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ETN 1978-12-07

NERVE LOCATER/STIMULATOR

Applicant Intermedics, Inc.

K-Number K781569

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EFQ 1978-12-07

BURN PAD, DRY, STERILE

Applicant Chesebrough-Pond'S U.S.A. Co.

K-Number K781985

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IMJ 1978-12-07

SIEMENS ULTRATHERM 708

Applicant Elmed, Inc.

K-Number K781455

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FPA 1978-12-07

I.V. SET WITH IN-LINE FILTER

Applicant Cutler Laboratories, Inc.

K-Number K781785

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FIL 1978-12-07

ULTRAFILTRATION SCALE

Applicant Extracorporeal Medical Specialities, Inc.

K-Number K781633

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KNX 1978-12-07

CATHETER, EXTERNAL MALE NURSING CARE

Applicant Medi-Tech, Inc.

K-Number K781780

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LAS 1978-12-07

THEOPHYLLINE CONTROL SERUM

Applicant Vitek Systems, Inc.

K-Number K780961

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KOH 1978-12-07

INSTRUMENT CURNETT MINI-CONER BIOPSY

Applicant C.R. Bard, Inc.

K-Number K781767

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