ISI FENESTRATED DISSECTING AND GRASPING FORCEPS
K-Number: K932534 · 1993-08-19
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Device Summary
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.
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
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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