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

KNT 1978-09-07

GAVAGE ADMIN. SET

Applicant Mcgaw Laboratories

K-Number K781230

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DPT 1978-09-07

MASK, PXYGEN

Applicant Vitalab Products Corp.

K-Number K781413

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ESD 1978-09-07

RADIOEAR RE SERIES HEARING AIDS

Applicant Radioear Corp.

K-Number K781458

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DJC 1978-09-07

CUTTER RESIFLEX FOLEY CATHETERS

Applicant Cutler Laboratories, Inc.

K-Number K781140

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KNX 1978-09-07

KWIK-FLO URINAL SYSTEM

Applicant The Grace Mfg. Co.

K-Number K781422

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HLM 1978-09-07

LENSOMETER MODEL 11

Applicant Rodenstock Instrument Corp.

K-Number K781440

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HKO 1978-09-07

AUTOREFRACTOR, SUBJECTIVE

Applicant Cavitron Corp.

K-Number K781014

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DXY 1978-09-07

PULSE GENERATOR MODEL 208

Applicant Elema-Schonander, Inc.

K-Number K781178

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DHN 1978-09-07

FLUORESCENT ANTI-NATIVE DNA TEST

Applicant Kallestad Laboratories, Inc.

K-Number K780899

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DXY 1978-09-07

CARDIAL PULSE GENERATORS

Applicant Telectronics, Inc.

K-Number K781426

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BTG 1978-09-07

CYTOLOGY BRUSH

Applicant CooperVision, Inc.

K-Number K780872

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DXY 1978-09-07

GENERATOR, CARDIAC PULSE, 250B

Applicant Telectronics, Inc.

K-Number K781090

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