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FDA 510(k)

ENDOSCOPES, FIBER OPTIC LAPAROSCOPES, (STERILIZABLE)

K-Number: K951482 · 1995-09-14

Decision Date1995-09-14
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPES, FIBER OPTIC LAPAROSCOPES, (STERILIZABLE) 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 1995-09-14 under 510(k) number K951482. 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 ENDOSCOPES, FIBER OPTIC LAPAROSCOPES, (STERILIZABLE)?

ENDOSCOPES, FIBER OPTIC LAPAROSCOPES, (STERILIZABLE) is a medical device that received FDA 510(k) clearance on 1995-09-14. The listed applicant is Micro-Medical Devices, Inc.. The 510(k) number is K951482.

When did ENDOSCOPES, FIBER OPTIC LAPAROSCOPES, (STERILIZABLE) receive FDA 510(k) clearance?

ENDOSCOPES, FIBER OPTIC LAPAROSCOPES, (STERILIZABLE) received FDA 510(k) clearance on 1995-09-14, under 510(k) number K951482.

Who is the listed applicant for ENDOSCOPES, FIBER OPTIC LAPAROSCOPES, (STERILIZABLE)?

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 ENDOSCOPES, FIBER OPTIC LAPAROSCOPES, (STERILIZABLE)?

The FDA product code for ENDOSCOPES, FIBER OPTIC LAPAROSCOPES, (STERILIZABLE) 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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