Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

AUTO SUTURE GAS POWERED DISP. LDS STAPL

K-Number: K810188 · 1981-03-20

Decision Date1981-03-20
Product CodeKBC
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

AUTO SUTURE GAS POWERED DISP. LDS STAPL 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 1981-03-20 under 510(k) number K810188. The device is classified under product code KBC. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO SUTURE GAS POWERED DISP. LDS STAPL?

AUTO SUTURE GAS POWERED DISP. LDS STAPL is a medical device that received FDA 510(k) clearance on 1981-03-20. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K810188.

When did AUTO SUTURE GAS POWERED DISP. LDS STAPL receive FDA 510(k) clearance?

AUTO SUTURE GAS POWERED DISP. LDS STAPL received FDA 510(k) clearance on 1981-03-20, under 510(k) number K810188.

Who is the listed applicant for AUTO SUTURE GAS POWERED DISP. LDS STAPL?

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 AUTO SUTURE GAS POWERED DISP. LDS STAPL?

The FDA product code for AUTO SUTURE GAS POWERED DISP. LDS STAPL is KBC.

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 United States Surgical, A Division of Tyco Healthc 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.

View all 218 devices →

Related Devices (Code: KBC)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑