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FDA 510(k)

ACE/KYLE SELF TAPPING CANNULATED TITA

K-Number: K833866 · 1983-12-27

ApplicantBuckman Co., Inc.
Decision Date1983-12-27
Product CodeJPW
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ACE/KYLE SELF TAPPING CANNULATED TITA is the device name listed in this FDA 510(k) record. The listed applicant is Buckman Co., Inc.. It received FDA 510(k) clearance on 1983-12-27 under 510(k) number K833866. The device is classified under product code JPW. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACE/KYLE SELF TAPPING CANNULATED TITA?

ACE/KYLE SELF TAPPING CANNULATED TITA is a medical device that received FDA 510(k) clearance on 1983-12-27. The listed applicant is Buckman Co., Inc.. The 510(k) number is K833866.

When did ACE/KYLE SELF TAPPING CANNULATED TITA receive FDA 510(k) clearance?

ACE/KYLE SELF TAPPING CANNULATED TITA received FDA 510(k) clearance on 1983-12-27, under 510(k) number K833866.

Who is the listed applicant for ACE/KYLE SELF TAPPING CANNULATED TITA?

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

What is the FDA product code for ACE/KYLE SELF TAPPING CANNULATED TITA?

The FDA product code for ACE/KYLE SELF TAPPING CANNULATED TITA is JPW.

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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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