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FDA 510(k)

HOOK PUNCH FORCEPS FOR ARTHROSCOPY

K-Number: K880331 · 1988-02-18

ApplicantKibbutz Gilgal Medical C/O Toam U.S.A. Corp.
Decision Date1988-02-18
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HOOK PUNCH FORCEPS FOR ARTHROSCOPY is the device name listed in this FDA 510(k) record. The listed applicant is Kibbutz Gilgal Medical C/O Toam U.S.A. Corp.. It received FDA 510(k) clearance on 1988-02-18 under 510(k) number K880331. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOOK PUNCH FORCEPS FOR ARTHROSCOPY?

HOOK PUNCH FORCEPS FOR ARTHROSCOPY is a medical device that received FDA 510(k) clearance on 1988-02-18. The listed applicant is Kibbutz Gilgal Medical C/O Toam U.S.A. Corp.. The 510(k) number is K880331.

When did HOOK PUNCH FORCEPS FOR ARTHROSCOPY receive FDA 510(k) clearance?

HOOK PUNCH FORCEPS FOR ARTHROSCOPY received FDA 510(k) clearance on 1988-02-18, under 510(k) number K880331.

Who is the listed applicant for HOOK PUNCH FORCEPS FOR ARTHROSCOPY?

The FDA 510(k) record lists Kibbutz Gilgal Medical C/O Toam U.S.A. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HOOK PUNCH FORCEPS FOR ARTHROSCOPY?

The FDA product code for HOOK PUNCH FORCEPS FOR ARTHROSCOPY is HRX.

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Related Devices (Code: HRX)

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Official Source

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

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