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FDA 510(k)

SCISSORS FOR LAPAROSCOPIC SURGERY OB/GYN USE

K-Number: K925957 · 1994-06-07

Decision Date1994-06-07
Product CodeHFI
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SCISSORS FOR LAPAROSCOPIC SURGERY OB/GYN USE 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 1994-06-07 under 510(k) number K925957. The device is classified under product code HFI. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCISSORS FOR LAPAROSCOPIC SURGERY OB/GYN USE?

SCISSORS FOR LAPAROSCOPIC SURGERY OB/GYN USE is a medical device that received FDA 510(k) clearance on 1994-06-07. The listed applicant is Zinnanti Surgical Instruments, Inc.. The 510(k) number is K925957.

When did SCISSORS FOR LAPAROSCOPIC SURGERY OB/GYN USE receive FDA 510(k) clearance?

SCISSORS FOR LAPAROSCOPIC SURGERY OB/GYN USE received FDA 510(k) clearance on 1994-06-07, under 510(k) number K925957.

Who is the listed applicant for SCISSORS FOR LAPAROSCOPIC SURGERY OB/GYN USE?

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 SCISSORS FOR LAPAROSCOPIC SURGERY OB/GYN USE?

The FDA product code for SCISSORS FOR LAPAROSCOPIC SURGERY OB/GYN USE is HFI.

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 Zinnanti Surgical Instruments, 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 76 devices →

Related Devices (Code: HFI)

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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