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FDA 510(k)

MIST SCISSORS FOR LAPAROSCOPIC/ENDOSCOPIC PROCEDUR

K-Number: K931272 · 1993-05-17

Decision Date1993-05-17
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MIST SCISSORS FOR LAPAROSCOPIC/ENDOSCOPIC PROCEDUR is the device name listed in this FDA 510(k) record. The listed applicant is Minimally Invasive Surgical Technologies, Inc.. It received FDA 510(k) clearance on 1993-05-17 under 510(k) number K931272. 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 MIST SCISSORS FOR LAPAROSCOPIC/ENDOSCOPIC PROCEDUR?

MIST SCISSORS FOR LAPAROSCOPIC/ENDOSCOPIC PROCEDUR is a medical device that received FDA 510(k) clearance on 1993-05-17. The listed applicant is Minimally Invasive Surgical Technologies, Inc.. The 510(k) number is K931272.

When did MIST SCISSORS FOR LAPAROSCOPIC/ENDOSCOPIC PROCEDUR receive FDA 510(k) clearance?

MIST SCISSORS FOR LAPAROSCOPIC/ENDOSCOPIC PROCEDUR received FDA 510(k) clearance on 1993-05-17, under 510(k) number K931272.

Who is the listed applicant for MIST SCISSORS FOR LAPAROSCOPIC/ENDOSCOPIC PROCEDUR?

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

What is the FDA product code for MIST SCISSORS FOR LAPAROSCOPIC/ENDOSCOPIC PROCEDUR?

The FDA product code for MIST SCISSORS FOR LAPAROSCOPIC/ENDOSCOPIC PROCEDUR is GCJ.

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 Minimally Invasive Surgical Technologies, 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: 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.

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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