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FDA 510(k)

LAPARAOSCOPES ELECTRONIC WITH STERILE SHEATH

K-Number: K940141 · 1994-05-19

Decision Date1994-05-19
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LAPARAOSCOPES ELECTRONIC WITH STERILE SHEATH is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Medical Devices, Inc.. It received FDA 510(k) clearance on 1994-05-19 under 510(k) number K940141. 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 LAPARAOSCOPES ELECTRONIC WITH STERILE SHEATH?

LAPARAOSCOPES ELECTRONIC WITH STERILE SHEATH is a medical device that received FDA 510(k) clearance on 1994-05-19. The listed applicant is Micro-Medical Devices, Inc.. The 510(k) number is K940141.

When did LAPARAOSCOPES ELECTRONIC WITH STERILE SHEATH receive FDA 510(k) clearance?

LAPARAOSCOPES ELECTRONIC WITH STERILE SHEATH received FDA 510(k) clearance on 1994-05-19, under 510(k) number K940141.

Who is the listed applicant for LAPARAOSCOPES ELECTRONIC WITH STERILE SHEATH?

The FDA 510(k) record lists Micro-Medical Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAPARAOSCOPES ELECTRONIC WITH STERILE SHEATH?

The FDA product code for LAPARAOSCOPES ELECTRONIC WITH STERILE SHEATH 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 Micro-Medical Devices, 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 8 devices →

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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