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FDA 510(k)

ETHICON MULTIPLE LIGATING CLIP APPLIER

K-Number: K812291 · 1981-09-11

ApplicantETHICON, Inc.
Decision Date1981-09-11
Product CodeGDO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ETHICON MULTIPLE LIGATING CLIP APPLIER is the device name listed in this FDA 510(k) record. The listed applicant is ETHICON, Inc.. It received FDA 510(k) clearance on 1981-09-11 under 510(k) number K812291. The device is classified under product code GDO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ETHICON MULTIPLE LIGATING CLIP APPLIER?

ETHICON MULTIPLE LIGATING CLIP APPLIER is a medical device that received FDA 510(k) clearance on 1981-09-11. The listed applicant is ETHICON, Inc.. The 510(k) number is K812291.

When did ETHICON MULTIPLE LIGATING CLIP APPLIER receive FDA 510(k) clearance?

ETHICON MULTIPLE LIGATING CLIP APPLIER received FDA 510(k) clearance on 1981-09-11, under 510(k) number K812291.

Who is the listed applicant for ETHICON MULTIPLE LIGATING CLIP APPLIER?

The FDA 510(k) record lists ETHICON, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ETHICON MULTIPLE LIGATING CLIP APPLIER?

The FDA product code for ETHICON MULTIPLE LIGATING CLIP APPLIER is GDO.

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Other records listing ETHICON, Inc. as applicant

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Related Devices (Code: GDO)

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.

K926199UNICLIP SURGICAL CLIP APPLIERUnisurge, Inc.K890941MODIFIED SUTURE DISP. ENDOSCOPIC SURGICAL CLIP APPUnited States Surgical, A Division of Tyco HealthcK890159TOWEL CLIPSDhason Brothers, Inc.K890233SUTURE CLIP APPLIER/REMOVERKinetic Medical ProductsK820837DISPOSABLE MULTIPLE LIGATING CLIPETHICON, Inc.K792378HEMOSPENSER CARTRIDGE CAT. NO. 523500-Edward Weck, 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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