FDA 510(k)

FOOT CONTROL PENCIL

K-Number: K926306 · 1993-02-05

ApplicantMegadyne Medical Products, Inc.

Decision Date1993-02-05

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

FOOT CONTROL PENCIL is the device name listed in this FDA 510(k) record. The listed applicant is Megadyne Medical Products, Inc.. It received FDA 510(k) clearance on 1993-02-05 under 510(k) number K926306. 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 FOOT CONTROL PENCIL?

FOOT CONTROL PENCIL is a medical device that received FDA 510(k) clearance on 1993-02-05. The listed applicant is Megadyne Medical Products, Inc.. The 510(k) number is K926306.

When did FOOT CONTROL PENCIL receive FDA 510(k) clearance?

FOOT CONTROL PENCIL received FDA 510(k) clearance on 1993-02-05, under 510(k) number K926306.

Who is the listed applicant for FOOT CONTROL PENCIL?

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

What is the FDA product code for FOOT CONTROL PENCIL?

The FDA product code for FOOT CONTROL PENCIL is GEI.

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Other records listing Megadyne Medical Products, Inc. as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.