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FDA 510(k)

HANDPIECE SHEATH-MODEL #A910

K-Number: K011929 · 2001-09-18

ApplicantAaron Medical, Inc.
Decision Date2001-09-18
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HANDPIECE SHEATH-MODEL #A910 is the device name listed in this FDA 510(k) record. The listed applicant is Aaron Medical, Inc.. It received FDA 510(k) clearance on 2001-09-18 under 510(k) number K011929. 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 HANDPIECE SHEATH-MODEL #A910?

HANDPIECE SHEATH-MODEL #A910 is a medical device that received FDA 510(k) clearance on 2001-09-18. The listed applicant is Aaron Medical, Inc.. The 510(k) number is K011929.

When did HANDPIECE SHEATH-MODEL #A910 receive FDA 510(k) clearance?

HANDPIECE SHEATH-MODEL #A910 received FDA 510(k) clearance on 2001-09-18, under 510(k) number K011929.

Who is the listed applicant for HANDPIECE SHEATH-MODEL #A910?

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

What is the FDA product code for HANDPIECE SHEATH-MODEL #A910?

The FDA product code for HANDPIECE SHEATH-MODEL #A910 is GEI.

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Other records listing Aaron Medical, Inc. as applicant

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Official Source

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