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FDA 510(k)

AESCULAP POWER SYSTEM HANDPIECE

K-Number: K960473 · 1996-03-07

ApplicantAesculap, Inc.
Decision Date1996-03-07
Product CodeGET
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AESCULAP POWER SYSTEM HANDPIECE is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 1996-03-07 under 510(k) number K960473. The device is classified under product code GET. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AESCULAP POWER SYSTEM HANDPIECE?

AESCULAP POWER SYSTEM HANDPIECE is a medical device that received FDA 510(k) clearance on 1996-03-07. The listed applicant is Aesculap, Inc.. The 510(k) number is K960473.

When did AESCULAP POWER SYSTEM HANDPIECE receive FDA 510(k) clearance?

AESCULAP POWER SYSTEM HANDPIECE received FDA 510(k) clearance on 1996-03-07, under 510(k) number K960473.

Who is the listed applicant for AESCULAP POWER SYSTEM HANDPIECE?

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 POWER SYSTEM HANDPIECE?

The FDA product code for AESCULAP POWER SYSTEM HANDPIECE is GET.

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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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