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FDA 510(k)

MODIFIED AUTO SUTURE PURSTRING DISP. AUTOMATIC

K-Number: K901107 · 1990-04-09

ApplicantUnited States Surgical, A Division of Tyco Healthc
Decision Date1990-04-09
Product CodeGDJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODIFIED AUTO SUTURE PURSTRING DISP. AUTOMATIC is the device name listed in this FDA 510(k) record. The listed applicant is United States Surgical, A Division of Tyco Healthc. It received FDA 510(k) clearance on 1990-04-09 under 510(k) number K901107. The device is classified under product code GDJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED AUTO SUTURE PURSTRING DISP. AUTOMATIC?

MODIFIED AUTO SUTURE PURSTRING DISP. AUTOMATIC is a medical device that received FDA 510(k) clearance on 1990-04-09. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K901107.

When did MODIFIED AUTO SUTURE PURSTRING DISP. AUTOMATIC receive FDA 510(k) clearance?

MODIFIED AUTO SUTURE PURSTRING DISP. AUTOMATIC received FDA 510(k) clearance on 1990-04-09, under 510(k) number K901107.

Who is the listed applicant for MODIFIED AUTO SUTURE PURSTRING DISP. AUTOMATIC?

The FDA 510(k) record lists United States Surgical, A Division of Tyco Healthc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED AUTO SUTURE PURSTRING DISP. AUTOMATIC?

The FDA product code for MODIFIED AUTO SUTURE PURSTRING DISP. AUTOMATIC is GDJ.

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Other records listing United States Surgical, A Division of Tyco Healthc as applicant

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Related Devices (Code: GDJ)

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.

K153358Standard ClampStandard BariatricsK930315THORACIC CLAMPS: SAROT, KANTOWITZ AND LAWRENCEThomasville Medical Assoc.K924223MAR-MED LIVER STRAPMar-Med Co.K922659GENERAL SURGERY CLAMP AND NEEDLE HOLDERMiltex Instrument Co.K914913GRICE FOOT PEDAL CONTROL/REDDICK IRRI/ASPIR SYSTIdeal Medical, Inc.K900956GS-7100 CHOLANGIOGRAM CLAMP, 5MMSolos Endoscopy, Inc.

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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