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FDA 510(k)

VERRESCOPE, LIGHT CABLE - LIGHT SOURCE ADAPTOR

K-Number: K971836 · 1997-11-07

ApplicantCooperSurgical, Inc.
Decision Date1997-11-07
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

VERRESCOPE, LIGHT CABLE - LIGHT SOURCE ADAPTOR is the device name listed in this FDA 510(k) record. The listed applicant is CooperSurgical, Inc.. It received FDA 510(k) clearance on 1997-11-07 under 510(k) number K971836. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERRESCOPE, LIGHT CABLE - LIGHT SOURCE ADAPTOR?

VERRESCOPE, LIGHT CABLE - LIGHT SOURCE ADAPTOR is a medical device that received FDA 510(k) clearance on 1997-11-07. The listed applicant is CooperSurgical, Inc.. The 510(k) number is K971836.

When did VERRESCOPE, LIGHT CABLE - LIGHT SOURCE ADAPTOR receive FDA 510(k) clearance?

VERRESCOPE, LIGHT CABLE - LIGHT SOURCE ADAPTOR received FDA 510(k) clearance on 1997-11-07, under 510(k) number K971836.

Who is the listed applicant for VERRESCOPE, LIGHT CABLE - LIGHT SOURCE ADAPTOR?

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

What is the FDA product code for VERRESCOPE, LIGHT CABLE - LIGHT SOURCE ADAPTOR?

The FDA product code for VERRESCOPE, LIGHT CABLE - LIGHT SOURCE ADAPTOR is HET.

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Related Devices (Code: HET)

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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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