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FDA 510(k)

PYTON

K-Number: K092733 · 2010-02-26

ApplicantArm Medical Devices, Inc.
Decision Date2010-02-26
Product CodeBSK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PYTON is the device name listed in this FDA 510(k) record. The listed applicant is Arm Medical Devices, Inc.. It received FDA 510(k) clearance on 2010-02-26 under 510(k) number K092733. The device is classified under product code BSK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PYTON?

PYTON is a medical device that received FDA 510(k) clearance on 2010-02-26. The listed applicant is Arm Medical Devices, Inc.. The 510(k) number is K092733.

When did PYTON receive FDA 510(k) clearance?

PYTON received FDA 510(k) clearance on 2010-02-26, under 510(k) number K092733.

Who is the listed applicant for PYTON?

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

What is the FDA product code for PYTON?

The FDA product code for PYTON is BSK.

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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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