FDA 510(k)

GRASPING FORCEP (W/FOUR PRONGS)

K-Number: K792100 · 1979-11-13

Decision Date1979-11-13

Product CodeGEN

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

GRASPING FORCEP (W/FOUR PRONGS) is the device name listed in this FDA 510(k) record. The listed applicant is Eder Instrument Co, Inc.. It received FDA 510(k) clearance on 1979-11-13 under 510(k) number K792100. The device is classified under product code GEN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRASPING FORCEP (W/FOUR PRONGS)?

GRASPING FORCEP (W/FOUR PRONGS) is a medical device that received FDA 510(k) clearance on 1979-11-13. The listed applicant is Eder Instrument Co, Inc.. The 510(k) number is K792100.

When did GRASPING FORCEP (W/FOUR PRONGS) receive FDA 510(k) clearance?

GRASPING FORCEP (W/FOUR PRONGS) received FDA 510(k) clearance on 1979-11-13, under 510(k) number K792100.

Who is the listed applicant for GRASPING FORCEP (W/FOUR PRONGS)?

The FDA 510(k) record lists Eder Instrument Co, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GRASPING FORCEP (W/FOUR PRONGS)?

The FDA product code for GRASPING FORCEP (W/FOUR PRONGS) is GEN.

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Other records listing Eder Instrument Co, Inc. as applicant

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Related Devices (Code: GEN)

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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.