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FDA 510(k)

LASSO (SCHWAITZBERG) SUTURE SNARE

K-Number: K934737 · 1994-03-09

Decision Date1994-03-09
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LASSO (SCHWAITZBERG) SUTURE SNARE is the device name listed in this FDA 510(k) record. The listed applicant is Performance Surgical Instruments Corp.. It received FDA 510(k) clearance on 1994-03-09 under 510(k) number K934737. 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 LASSO (SCHWAITZBERG) SUTURE SNARE?

LASSO (SCHWAITZBERG) SUTURE SNARE is a medical device that received FDA 510(k) clearance on 1994-03-09. The listed applicant is Performance Surgical Instruments Corp.. The 510(k) number is K934737.

When did LASSO (SCHWAITZBERG) SUTURE SNARE receive FDA 510(k) clearance?

LASSO (SCHWAITZBERG) SUTURE SNARE received FDA 510(k) clearance on 1994-03-09, under 510(k) number K934737.

Who is the listed applicant for LASSO (SCHWAITZBERG) SUTURE SNARE?

The FDA 510(k) record lists Performance Surgical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LASSO (SCHWAITZBERG) SUTURE SNARE?

The FDA product code for LASSO (SCHWAITZBERG) SUTURE SNARE is GCJ.

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 Performance Surgical Instruments Corp. 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.

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.

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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