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FDA 510(k)

SLIMLINE SURGICAL CLAMP; SLIMLINE JAW INSERTS

K-Number: K992640 · 1999-09-08

ApplicantMinumys Surgical, Inc.
Decision Date1999-09-08
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SLIMLINE SURGICAL CLAMP; SLIMLINE JAW INSERTS is the device name listed in this FDA 510(k) record. The listed applicant is Minumys Surgical, Inc.. It received FDA 510(k) clearance on 1999-09-08 under 510(k) number K992640. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SLIMLINE SURGICAL CLAMP; SLIMLINE JAW INSERTS?

SLIMLINE SURGICAL CLAMP; SLIMLINE JAW INSERTS is a medical device that received FDA 510(k) clearance on 1999-09-08. The listed applicant is Minumys Surgical, Inc.. The 510(k) number is K992640.

When did SLIMLINE SURGICAL CLAMP; SLIMLINE JAW INSERTS receive FDA 510(k) clearance?

SLIMLINE SURGICAL CLAMP; SLIMLINE JAW INSERTS received FDA 510(k) clearance on 1999-09-08, under 510(k) number K992640.

Who is the listed applicant for SLIMLINE SURGICAL CLAMP; SLIMLINE JAW INSERTS?

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

What is the FDA product code for SLIMLINE SURGICAL CLAMP; SLIMLINE JAW INSERTS?

The FDA product code for SLIMLINE SURGICAL CLAMP; SLIMLINE JAW INSERTS is DXC.

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Related Devices (Code: DXC)

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

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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