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FDA 510(k)

ISI FENESTRATED DISSECTING AND GRASPING FORCEPS

K-Number: K932534 · 1993-08-19

Decision Date1993-08-19
Product CodeGFI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ISI FENESTRATED DISSECTING AND GRASPING FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Surgical, Inc.. It received FDA 510(k) clearance on 1993-08-19 under 510(k) number K932534. The device is classified under product code GFI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ISI FENESTRATED DISSECTING AND GRASPING FORCEPS?

ISI FENESTRATED DISSECTING AND GRASPING FORCEPS is a medical device that received FDA 510(k) clearance on 1993-08-19. The listed applicant is Innovative Surgical, Inc.. The 510(k) number is K932534.

When did ISI FENESTRATED DISSECTING AND GRASPING FORCEPS receive FDA 510(k) clearance?

ISI FENESTRATED DISSECTING AND GRASPING FORCEPS received FDA 510(k) clearance on 1993-08-19, under 510(k) number K932534.

Who is the listed applicant for ISI FENESTRATED DISSECTING AND GRASPING FORCEPS?

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

What is the FDA product code for ISI FENESTRATED DISSECTING AND GRASPING FORCEPS?

The FDA product code for ISI FENESTRATED DISSECTING AND GRASPING FORCEPS is GFI.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Innovative Surgical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 7 devices →

Related Devices (Code: GFI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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