SCISSORS FOR LAPAROSCOPIC SURGERY OB/GYN USE
K-Number: K925957 · 1994-06-07
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Device Summary
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.
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
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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