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FDA 510(k)

AUTO SUTURE(R) ENDOSCOPIC CLAMP

K-Number: K903205 · 1990-10-11

ApplicantUnited States Surgical, A Division of Tyco Healthc
Decision Date1990-10-11
Product CodeHDA
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

AUTO SUTURE(R) ENDOSCOPIC CLAMP 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 1990-10-11 under 510(k) number K903205. The device is classified under product code HDA. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO SUTURE(R) ENDOSCOPIC CLAMP?

AUTO SUTURE(R) ENDOSCOPIC CLAMP is a medical device that received FDA 510(k) clearance on 1990-10-11. The listed applicant is United States Surgical, A Division of Tyco Healthc. The 510(k) number is K903205.

When did AUTO SUTURE(R) ENDOSCOPIC CLAMP receive FDA 510(k) clearance?

AUTO SUTURE(R) ENDOSCOPIC CLAMP received FDA 510(k) clearance on 1990-10-11, under 510(k) number K903205.

Who is the listed applicant for AUTO SUTURE(R) ENDOSCOPIC CLAMP?

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(R) ENDOSCOPIC CLAMP?

The FDA product code for AUTO SUTURE(R) ENDOSCOPIC CLAMP is HDA.

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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.

K071406AUTOSUTURE ENDO CLIP III 5 MM CLIP APPLIERK071920AUTOSUTURE ABSORBABLE TACK AND APPLICATORK061288AUTO SUTURE ENDO CLIP III 5 MM CLIP APPLIERK062850AUTOSUTURE CIRCULAR EEA SURGICAL STAPLERSK062326AUTOSUTURE MODIFIED VERSAPORT TROCAR WITH FIXATION SLEEVEK061095AUTO SUTUR ENDO GIA STAPLERS

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Related Devices (Code: HDA)

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.

K100517INSTRUMED FORCEPS OBSTERICAL, MODEL# 46-5XXX, OB-XXXXInstrumed International, Inc.K092827DIMELA OBSTERICAL FORCEPS, MODEL 72.1 XX XXDimeda Instrumente GmbHK013747TEKNO-MEDICAL OBSTETRICAL FORCEPSTekno Medical Optik-Chirurgie GmbH & Co.K951529V. MUELLER OBSTETRICAL (OB) FORCEPSBaxter Healthcare CorpK914552CMI VACUUM PUMPColumbia Medical & Surgical, Inc.K905583ILC FORCEPS PADSInman Liebelt Corp.

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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