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FDA 510(k)

BISURE LAPAROSCOPIC BIPOLAR FORCEPS

K-Number: K983743 · 1999-01-21

ApplicantValleylab, Inc.
Decision Date1999-01-21
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BISURE LAPAROSCOPIC BIPOLAR FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1999-01-21 under 510(k) number K983743. 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 BISURE LAPAROSCOPIC BIPOLAR FORCEPS?

BISURE LAPAROSCOPIC BIPOLAR FORCEPS is a medical device that received FDA 510(k) clearance on 1999-01-21. The listed applicant is Valleylab, Inc.. The 510(k) number is K983743.

When did BISURE LAPAROSCOPIC BIPOLAR FORCEPS receive FDA 510(k) clearance?

BISURE LAPAROSCOPIC BIPOLAR FORCEPS received FDA 510(k) clearance on 1999-01-21, under 510(k) number K983743.

Who is the listed applicant for BISURE LAPAROSCOPIC BIPOLAR FORCEPS?

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

What is the FDA product code for BISURE LAPAROSCOPIC BIPOLAR FORCEPS?

The FDA product code for BISURE LAPAROSCOPIC BIPOLAR FORCEPS is GEI.

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Other records listing Valleylab, 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.

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Related Devices (Code: GEI)

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.

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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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