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FDA 510(k)

PERICSCOPE, MODEL # PERISC1

K-Number: K013576 · 2002-01-25

ApplicantEthicon Endo-Surgery, Inc.
Decision Date2002-01-25
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PERICSCOPE, MODEL # PERISC1 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 2002-01-25 under 510(k) number K013576. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERICSCOPE, MODEL # PERISC1?

PERICSCOPE, MODEL # PERISC1 is a medical device that received FDA 510(k) clearance on 2002-01-25. The listed applicant is Ethicon Endo-Surgery, Inc.. The 510(k) number is K013576.

When did PERICSCOPE, MODEL # PERISC1 receive FDA 510(k) clearance?

PERICSCOPE, MODEL # PERISC1 received FDA 510(k) clearance on 2002-01-25, under 510(k) number K013576.

Who is the listed applicant for PERICSCOPE, MODEL # PERISC1?

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 PERICSCOPE, MODEL # PERISC1?

The FDA product code for PERICSCOPE, MODEL # PERISC1 is GCJ.

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Related Devices (Code: GCJ)

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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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