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FDA 510(k)

MENTOR WET-FIELD*II COAGULATOR

K-Number: K881001 · 1988-05-13

Decision Date1988-05-13
Product CodeHQQ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MENTOR WET-FIELD*II COAGULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Mentor O & O, Inc.. It received FDA 510(k) clearance on 1988-05-13 under 510(k) number K881001. The device is classified under product code HQQ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MENTOR WET-FIELD*II COAGULATOR?

MENTOR WET-FIELD*II COAGULATOR is a medical device that received FDA 510(k) clearance on 1988-05-13. The listed applicant is Mentor O & O, Inc.. The 510(k) number is K881001.

When did MENTOR WET-FIELD*II COAGULATOR receive FDA 510(k) clearance?

MENTOR WET-FIELD*II COAGULATOR received FDA 510(k) clearance on 1988-05-13, under 510(k) number K881001.

Who is the listed applicant for MENTOR WET-FIELD*II COAGULATOR?

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

What is the FDA product code for MENTOR WET-FIELD*II COAGULATOR?

The FDA product code for MENTOR WET-FIELD*II COAGULATOR is HQQ.

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 Mentor O & O, 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.

View all 18 devices →

Related Devices (Code: HQQ)

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

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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