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FDA 510(k)

INSTRUMENTS FOR ENDOSCOPIC PLASTIC SURGERY (EPS)

K-Number: K980129 · 1998-11-05

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date1998-11-05
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INSTRUMENTS FOR ENDOSCOPIC PLASTIC SURGERY (EPS) is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 1998-11-05 under 510(k) number K980129. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTRUMENTS FOR ENDOSCOPIC PLASTIC SURGERY (EPS)?

INSTRUMENTS FOR ENDOSCOPIC PLASTIC SURGERY (EPS) is a medical device that received FDA 510(k) clearance on 1998-11-05. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K980129.

When did INSTRUMENTS FOR ENDOSCOPIC PLASTIC SURGERY (EPS) receive FDA 510(k) clearance?

INSTRUMENTS FOR ENDOSCOPIC PLASTIC SURGERY (EPS) received FDA 510(k) clearance on 1998-11-05, under 510(k) number K980129.

Who is the listed applicant for INSTRUMENTS FOR ENDOSCOPIC PLASTIC SURGERY (EPS)?

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

What is the FDA product code for INSTRUMENTS FOR ENDOSCOPIC PLASTIC SURGERY (EPS)?

The FDA product code for INSTRUMENTS FOR ENDOSCOPIC PLASTIC SURGERY (EPS) is GCJ.

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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.

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