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FDA 510(k)

BATTERY POWERED ENDOSCCOPIC LIGHT SOURCE

K-Number: K960081 · 1996-03-12

ApplicantMitsubishi Cable America, Inc.
Decision Date1996-03-12
Product CodeFCQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BATTERY POWERED ENDOSCCOPIC LIGHT SOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Mitsubishi Cable America, Inc.. It received FDA 510(k) clearance on 1996-03-12 under 510(k) number K960081. The device is classified under product code FCQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BATTERY POWERED ENDOSCCOPIC LIGHT SOURCE?

BATTERY POWERED ENDOSCCOPIC LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 1996-03-12. The listed applicant is Mitsubishi Cable America, Inc.. The 510(k) number is K960081.

When did BATTERY POWERED ENDOSCCOPIC LIGHT SOURCE receive FDA 510(k) clearance?

BATTERY POWERED ENDOSCCOPIC LIGHT SOURCE received FDA 510(k) clearance on 1996-03-12, under 510(k) number K960081.

Who is the listed applicant for BATTERY POWERED ENDOSCCOPIC LIGHT SOURCE?

The FDA 510(k) record lists Mitsubishi Cable America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BATTERY POWERED ENDOSCCOPIC LIGHT SOURCE?

The FDA product code for BATTERY POWERED ENDOSCCOPIC LIGHT SOURCE is FCQ.

Related Clinical Trials

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Other records listing Mitsubishi Cable America, 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.

K955717ENDOSCOPE INTRODUCER KITK936257ULTRATHIN FLEXIBLE ENDOSCOPE TAS-211/2.3

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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