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FDA 510(k)

DANNINGER TRIMCHECK(TM) PORTABLE & DESK TOP MODELS

K-Number: K881841 · 1988-12-13

ApplicantBuckman Co., Inc.
Decision Date1988-12-13
Product CodeDSB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DANNINGER TRIMCHECK(TM) PORTABLE & DESK TOP MODELS 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 1988-12-13 under 510(k) number K881841. The device is classified under product code DSB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DANNINGER TRIMCHECK(TM) PORTABLE & DESK TOP MODELS?

DANNINGER TRIMCHECK(TM) PORTABLE & DESK TOP MODELS is a medical device that received FDA 510(k) clearance on 1988-12-13. The listed applicant is Buckman Co., Inc.. The 510(k) number is K881841.

When did DANNINGER TRIMCHECK(TM) PORTABLE & DESK TOP MODELS receive FDA 510(k) clearance?

DANNINGER TRIMCHECK(TM) PORTABLE & DESK TOP MODELS received FDA 510(k) clearance on 1988-12-13, under 510(k) number K881841.

Who is the listed applicant for DANNINGER TRIMCHECK(TM) PORTABLE & DESK TOP MODELS?

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 DANNINGER TRIMCHECK(TM) PORTABLE & DESK TOP MODELS?

The FDA product code for DANNINGER TRIMCHECK(TM) PORTABLE & DESK TOP MODELS is DSB.

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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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