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FDA 510(k)

ENDOPATH TISSUE RETAINING COMPONENT

K-Number: K923679 · 1992-09-09

ApplicantEthicon Endo-Surgery, Inc.
Decision Date1992-09-09
Product CodeKCJ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ENDOPATH TISSUE RETAINING COMPONENT is the device name listed in this FDA 510(k) record. The listed applicant is Ethicon Endo-Surgery, Inc.. It received FDA 510(k) clearance on 1992-09-09 under 510(k) number K923679. The device is classified under product code KCJ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOPATH TISSUE RETAINING COMPONENT?

ENDOPATH TISSUE RETAINING COMPONENT is a medical device that received FDA 510(k) clearance on 1992-09-09. The listed applicant is Ethicon Endo-Surgery, Inc.. The 510(k) number is K923679.

When did ENDOPATH TISSUE RETAINING COMPONENT receive FDA 510(k) clearance?

ENDOPATH TISSUE RETAINING COMPONENT received FDA 510(k) clearance on 1992-09-09, under 510(k) number K923679.

Who is the listed applicant for ENDOPATH TISSUE RETAINING COMPONENT?

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

What is the FDA product code for ENDOPATH TISSUE RETAINING COMPONENT?

The FDA product code for ENDOPATH TISSUE RETAINING COMPONENT is KCJ.

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Other records listing Ethicon Endo-Surgery, Inc. 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.

K111195VALUTRUS REUSABLE CIRCULAR STAPLER AND DISPOSABLE RELOADSK110385ECHELON FLEX 45 / 60 POWERED ARTICULATING ENDOSCOPIC LINEAR CUTTERK101520ENSEAL TISSUE SEALING DEVICES MODEL: NSEAL514H-535H, NSEAL514RH-535RHK102632ETHICON ENDO-SURGERY 5MM LAPAROSCOPIC MULTI-FEED STAPLERK093896ETHICON ENDO SURGERY SLOTTED ANOSCOPEK091259ETHICON ENDO-SURGERY FLEXIBLE BIPOLAR HEMOSTASIS FORCEPS

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Related Devices (Code: KCJ)

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.

K921053LAPAROMED LIGATING LOOPLaparomed Corp.K894369APDYNE PHENOL APPLICATOR KITApdyne Medical Co.K832667LUCAE'S EAR & NASAL APPLICATORSKells Medical, 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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