ENDOPATH II DISPOSABLE SURGICAL TROCAR & SLEEVE
K-Number: K932282 · 1993-06-22
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Device Summary
Frequently Asked Questions
What is the ENDOPATH II DISPOSABLE SURGICAL TROCAR & SLEEVE?
ENDOPATH II DISPOSABLE SURGICAL TROCAR & SLEEVE is a medical device that received FDA 510(k) clearance on 1993-06-22. The listed applicant is Ethicon Endo-Surgery, Inc.. The 510(k) number is K932282.
When did ENDOPATH II DISPOSABLE SURGICAL TROCAR & SLEEVE receive FDA 510(k) clearance?
ENDOPATH II DISPOSABLE SURGICAL TROCAR & SLEEVE received FDA 510(k) clearance on 1993-06-22, under 510(k) number K932282.
Who is the listed applicant for ENDOPATH II DISPOSABLE SURGICAL TROCAR & SLEEVE?
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 II DISPOSABLE SURGICAL TROCAR & SLEEVE?
The FDA product code for ENDOPATH II DISPOSABLE SURGICAL TROCAR & SLEEVE is GCJ.
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 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.
Related Devices (Code: GCJ)
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.
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