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FDA 510(k)

BEND-A-BEAM HAND CONTROL MALLEABLE ABC HANDPIECE

K-Number: K961505 · 1996-07-18

ApplicantConmedcorp
Decision Date1996-07-18
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BEND-A-BEAM HAND CONTROL MALLEABLE ABC HANDPIECE is the device name listed in this FDA 510(k) record. The listed applicant is Conmedcorp. It received FDA 510(k) clearance on 1996-07-18 under 510(k) number K961505. 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 BEND-A-BEAM HAND CONTROL MALLEABLE ABC HANDPIECE?

BEND-A-BEAM HAND CONTROL MALLEABLE ABC HANDPIECE is a medical device that received FDA 510(k) clearance on 1996-07-18. The listed applicant is Conmedcorp. The 510(k) number is K961505.

When did BEND-A-BEAM HAND CONTROL MALLEABLE ABC HANDPIECE receive FDA 510(k) clearance?

BEND-A-BEAM HAND CONTROL MALLEABLE ABC HANDPIECE received FDA 510(k) clearance on 1996-07-18, under 510(k) number K961505.

Who is the listed applicant for BEND-A-BEAM HAND CONTROL MALLEABLE ABC HANDPIECE?

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

What is the FDA product code for BEND-A-BEAM HAND CONTROL MALLEABLE ABC HANDPIECE?

The FDA product code for BEND-A-BEAM HAND CONTROL MALLEABLE ABC HANDPIECE is GEI.

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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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