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FDA 510(k)

CIRCON ACMI GEN SURG INSTRU FOR MINI INVASIVE SURG

K-Number: K914883 · 1993-01-15

ApplicantCircon Video
Decision Date1993-01-15
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CIRCON ACMI GEN SURG INSTRU FOR MINI INVASIVE SURG is the device name listed in this FDA 510(k) record. The listed applicant is Circon Video. It received FDA 510(k) clearance on 1993-01-15 under 510(k) number K914883. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CIRCON ACMI GEN SURG INSTRU FOR MINI INVASIVE SURG?

CIRCON ACMI GEN SURG INSTRU FOR MINI INVASIVE SURG is a medical device that received FDA 510(k) clearance on 1993-01-15. The listed applicant is Circon Video. The 510(k) number is K914883.

When did CIRCON ACMI GEN SURG INSTRU FOR MINI INVASIVE SURG receive FDA 510(k) clearance?

CIRCON ACMI GEN SURG INSTRU FOR MINI INVASIVE SURG received FDA 510(k) clearance on 1993-01-15, under 510(k) number K914883.

Who is the listed applicant for CIRCON ACMI GEN SURG INSTRU FOR MINI INVASIVE SURG?

The FDA 510(k) record lists Circon Video as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CIRCON ACMI GEN SURG INSTRU FOR MINI INVASIVE SURG?

The FDA product code for CIRCON ACMI GEN SURG INSTRU FOR MINI INVASIVE SURG is GEI.

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Other records listing Circon Video as applicant

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Related Devices (Code: GEI)

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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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