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FDA 510(k)

E-TYPE STRAIGHT HANDPIECE, MODEL AHP-101

K-Number: K051077 · 2005-05-03

ApplicantAseptico, Inc.
Decision Date2005-05-03
Product CodeEGS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

E-TYPE STRAIGHT HANDPIECE, MODEL AHP-101 is the device name listed in this FDA 510(k) record. The listed applicant is Aseptico, Inc.. It received FDA 510(k) clearance on 2005-05-03 under 510(k) number K051077. The device is classified under product code EGS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the E-TYPE STRAIGHT HANDPIECE, MODEL AHP-101?

E-TYPE STRAIGHT HANDPIECE, MODEL AHP-101 is a medical device that received FDA 510(k) clearance on 2005-05-03. The listed applicant is Aseptico, Inc.. The 510(k) number is K051077.

When did E-TYPE STRAIGHT HANDPIECE, MODEL AHP-101 receive FDA 510(k) clearance?

E-TYPE STRAIGHT HANDPIECE, MODEL AHP-101 received FDA 510(k) clearance on 2005-05-03, under 510(k) number K051077.

Who is the listed applicant for E-TYPE STRAIGHT HANDPIECE, MODEL AHP-101?

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

What is the FDA product code for E-TYPE STRAIGHT HANDPIECE, MODEL AHP-101?

The FDA product code for E-TYPE STRAIGHT HANDPIECE, MODEL AHP-101 is EGS.

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Related Devices (Code: EGS)

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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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