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FDA 510(k)

ZSI LAPAROSCOPES-GENERAL & PLASTIC SURGERY

K-Number: K926181 · 1993-12-17

ApplicantZinnanti Surgical Instruments, Inc.
Decision Date1993-12-17
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ZSI LAPAROSCOPES-GENERAL & PLASTIC SURGERY is the device name listed in this FDA 510(k) record. The listed applicant is Zinnanti Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1993-12-17 under 510(k) number K926181. 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 ZSI LAPAROSCOPES-GENERAL & PLASTIC SURGERY?

ZSI LAPAROSCOPES-GENERAL & PLASTIC SURGERY is a medical device that received FDA 510(k) clearance on 1993-12-17. The listed applicant is Zinnanti Surgical Instruments, Inc.. The 510(k) number is K926181.

When did ZSI LAPAROSCOPES-GENERAL & PLASTIC SURGERY receive FDA 510(k) clearance?

ZSI LAPAROSCOPES-GENERAL & PLASTIC SURGERY received FDA 510(k) clearance on 1993-12-17, under 510(k) number K926181.

Who is the listed applicant for ZSI LAPAROSCOPES-GENERAL & PLASTIC SURGERY?

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

What is the FDA product code for ZSI LAPAROSCOPES-GENERAL & PLASTIC SURGERY?

The FDA product code for ZSI LAPAROSCOPES-GENERAL & PLASTIC SURGERY is GCJ.

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Other records listing Zinnanti Surgical Instruments, Inc. as applicant

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Related Devices (Code: GCJ)

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.

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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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