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FDA 510(k)

ENDOSCOPIC CLIP APPLIER

K-Number: K962493 · 1996-09-11

ApplicantAesculap, Inc.
Decision Date1996-09-11
Product CodeOCW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPIC CLIP APPLIER is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 1996-09-11 under 510(k) number K962493. The device is classified under product code OCW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSCOPIC CLIP APPLIER?

ENDOSCOPIC CLIP APPLIER is a medical device that received FDA 510(k) clearance on 1996-09-11. The listed applicant is Aesculap, Inc.. The 510(k) number is K962493.

When did ENDOSCOPIC CLIP APPLIER receive FDA 510(k) clearance?

ENDOSCOPIC CLIP APPLIER received FDA 510(k) clearance on 1996-09-11, under 510(k) number K962493.

Who is the listed applicant for ENDOSCOPIC CLIP APPLIER?

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

What is the FDA product code for ENDOSCOPIC CLIP APPLIER?

The FDA product code for ENDOSCOPIC CLIP APPLIER is OCW.

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Other records listing Aesculap, 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.

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Related Devices (Code: OCW)

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.

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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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