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FDA 510(k)

FIBER OPTIC UNIVERAL CABLES, SCOPE ADAP., LT.SOURC

K-Number: K912767 · 1991-08-13

Decision Date1991-08-13
Product CodeEQH
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

FIBER OPTIC UNIVERAL CABLES, SCOPE ADAP., LT.SOURC is the device name listed in this FDA 510(k) record. The listed applicant is Microaire Advanced Surgical Products. It received FDA 510(k) clearance on 1991-08-13 under 510(k) number K912767. The device is classified under product code EQH. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIBER OPTIC UNIVERAL CABLES, SCOPE ADAP., LT.SOURC?

FIBER OPTIC UNIVERAL CABLES, SCOPE ADAP., LT.SOURC is a medical device that received FDA 510(k) clearance on 1991-08-13. The listed applicant is Microaire Advanced Surgical Products. The 510(k) number is K912767.

When did FIBER OPTIC UNIVERAL CABLES, SCOPE ADAP., LT.SOURC receive FDA 510(k) clearance?

FIBER OPTIC UNIVERAL CABLES, SCOPE ADAP., LT.SOURC received FDA 510(k) clearance on 1991-08-13, under 510(k) number K912767.

Who is the listed applicant for FIBER OPTIC UNIVERAL CABLES, SCOPE ADAP., LT.SOURC?

The FDA 510(k) record lists Microaire Advanced Surgical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FIBER OPTIC UNIVERAL CABLES, SCOPE ADAP., LT.SOURC?

The FDA product code for FIBER OPTIC UNIVERAL CABLES, SCOPE ADAP., LT.SOURC is EQH.

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 Microaire Advanced Surgical Products 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: EQH)

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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