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FDA 510(k)

UNIFLEX DANNINGER

K-Number: K843309 · 1984-10-16

ApplicantBuckman Co., Inc.
Decision Date1984-10-16
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

UNIFLEX DANNINGER 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 1984-10-16 under 510(k) number K843309. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIFLEX DANNINGER?

UNIFLEX DANNINGER is a medical device that received FDA 510(k) clearance on 1984-10-16. The listed applicant is Buckman Co., Inc.. The 510(k) number is K843309.

When did UNIFLEX DANNINGER receive FDA 510(k) clearance?

UNIFLEX DANNINGER received FDA 510(k) clearance on 1984-10-16, under 510(k) number K843309.

Who is the listed applicant for UNIFLEX DANNINGER?

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 UNIFLEX DANNINGER?

The FDA product code for UNIFLEX DANNINGER is BXB.

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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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