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FDA 510(k)

AESCULAP MANUAL ENDOSCOPIC INSTRUMENTS

K-Number: K922576 · 1993-06-10

ApplicantAesculap, Inc.
Decision Date1993-06-10
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AESCULAP MANUAL ENDOSCOPIC INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 1993-06-10 under 510(k) number K922576. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AESCULAP MANUAL ENDOSCOPIC INSTRUMENTS?

AESCULAP MANUAL ENDOSCOPIC INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1993-06-10. The listed applicant is Aesculap, Inc.. The 510(k) number is K922576.

When did AESCULAP MANUAL ENDOSCOPIC INSTRUMENTS receive FDA 510(k) clearance?

AESCULAP MANUAL ENDOSCOPIC INSTRUMENTS received FDA 510(k) clearance on 1993-06-10, under 510(k) number K922576.

Who is the listed applicant for AESCULAP MANUAL ENDOSCOPIC INSTRUMENTS?

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 AESCULAP MANUAL ENDOSCOPIC INSTRUMENTS?

The FDA product code for AESCULAP MANUAL ENDOSCOPIC INSTRUMENTS is GEI.

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Other records listing Aesculap, Inc. as applicant

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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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