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FDA 510(k)

AESCULAP LAPAROSCOPIC ANCILLARY DEVICES

K-Number: K943603 · 1995-03-29

ApplicantAesculap, Inc.
Decision Date1995-03-29
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

AESCULAP LAPAROSCOPIC ANCILLARY DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 1995-03-29 under 510(k) number K943603. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AESCULAP LAPAROSCOPIC ANCILLARY DEVICES?

AESCULAP LAPAROSCOPIC ANCILLARY DEVICES is a medical device that received FDA 510(k) clearance on 1995-03-29. The listed applicant is Aesculap, Inc.. The 510(k) number is K943603.

When did AESCULAP LAPAROSCOPIC ANCILLARY DEVICES receive FDA 510(k) clearance?

AESCULAP LAPAROSCOPIC ANCILLARY DEVICES received FDA 510(k) clearance on 1995-03-29, under 510(k) number K943603.

Who is the listed applicant for AESCULAP LAPAROSCOPIC ANCILLARY DEVICES?

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 LAPAROSCOPIC ANCILLARY DEVICES?

The FDA product code for AESCULAP LAPAROSCOPIC ANCILLARY DEVICES is HET.

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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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