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FDA 510(k)

CANUSEAL

K-Number: K925932 · 1993-04-23

ApplicantLap Associates of Nashville, Ii, Inc.
Decision Date1993-04-23
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CANUSEAL is the device name listed in this FDA 510(k) record. The listed applicant is Lap Associates of Nashville, Ii, Inc.. It received FDA 510(k) clearance on 1993-04-23 under 510(k) number K925932. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANUSEAL?

CANUSEAL is a medical device that received FDA 510(k) clearance on 1993-04-23. The listed applicant is Lap Associates of Nashville, Ii, Inc.. The 510(k) number is K925932.

When did CANUSEAL receive FDA 510(k) clearance?

CANUSEAL received FDA 510(k) clearance on 1993-04-23, under 510(k) number K925932.

Who is the listed applicant for CANUSEAL?

The FDA 510(k) record lists Lap Associates of Nashville, Ii, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CANUSEAL?

The FDA product code for CANUSEAL is GCJ.

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Related Devices (Code: GCJ)

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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