FDA 510(k)

KITTNER DISSECTOR

K-Number: K953059 · 1995-09-14

Decision Date1995-09-14

Product CodeGDY

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

KITTNER DISSECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Medical Perspectives Corp.. It received FDA 510(k) clearance on 1995-09-14 under 510(k) number K953059. The device is classified under product code GDY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KITTNER DISSECTOR?

KITTNER DISSECTOR is a medical device that received FDA 510(k) clearance on 1995-09-14. The listed applicant is Medical Perspectives Corp.. The 510(k) number is K953059.

When did KITTNER DISSECTOR receive FDA 510(k) clearance?

KITTNER DISSECTOR received FDA 510(k) clearance on 1995-09-14, under 510(k) number K953059.

Who is the listed applicant for KITTNER DISSECTOR?

The FDA 510(k) record lists Medical Perspectives Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KITTNER DISSECTOR?

The FDA product code for KITTNER DISSECTOR is GDY.

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Other records listing Medical Perspectives Corp. as applicant

K953060ROSEBUD DISSECTOR K953058ROUND STICK SPONGES, FLAT STICK SPONGES K953088TRIANGULAR SPONGES K953057CYLINDRICAL SPONGE K953087CHERRY PIT DISSECTOR K953062CHERRY DISSECTOR

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Related Devices (Code: GDY)

K972634ULTRACELL SUCTION SPONGEUltracell Medical Technologies, Inc.K960236CPR LAP SPONGESCustom Pack Reliability K955599STRYKER FEMORAL CANAL SPONGE & ACETABULUM SPONGEStryker Corp.K955322PROTEC X-RAY DETECTABLE GAUZE SPONGEDerivados DE Gasa, S.A. DE C.V.K953830KENSORBKentron Health Care, Inc.K953058ROUND STICK SPONGES, FLAT STICK SPONGESMedical Perspectives Corp.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.