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FDA 510(k)

INSIGHT 4000 ENDOSCOPE

K-Number: K000252 · 2000-10-17

ApplicantInsight Instruments Mfg., Inc.
Decision Date2000-10-17
Product CodeMPA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INSIGHT 4000 ENDOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Insight Instruments Mfg., Inc.. It received FDA 510(k) clearance on 2000-10-17 under 510(k) number K000252. The device is classified under product code MPA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSIGHT 4000 ENDOSCOPE?

INSIGHT 4000 ENDOSCOPE is a medical device that received FDA 510(k) clearance on 2000-10-17. The listed applicant is Insight Instruments Mfg., Inc.. The 510(k) number is K000252.

When did INSIGHT 4000 ENDOSCOPE receive FDA 510(k) clearance?

INSIGHT 4000 ENDOSCOPE received FDA 510(k) clearance on 2000-10-17, under 510(k) number K000252.

Who is the listed applicant for INSIGHT 4000 ENDOSCOPE?

The FDA 510(k) record lists Insight Instruments Mfg., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSIGHT 4000 ENDOSCOPE?

The FDA product code for INSIGHT 4000 ENDOSCOPE is MPA.

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Related Devices (Code: MPA)

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.

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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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