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FDA 510(k)

COMFORTWEIGH

K-Number: K871771 · 1987-06-24

ApplicantCurlington Industrial Electronics, Inc.
Decision Date1987-06-24
Product CodeFRW
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

COMFORTWEIGH is the device name listed in this FDA 510(k) record. The listed applicant is Curlington Industrial Electronics, Inc.. It received FDA 510(k) clearance on 1987-06-24 under 510(k) number K871771. The device is classified under product code FRW. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMFORTWEIGH?

COMFORTWEIGH is a medical device that received FDA 510(k) clearance on 1987-06-24. The listed applicant is Curlington Industrial Electronics, Inc.. The 510(k) number is K871771.

When did COMFORTWEIGH receive FDA 510(k) clearance?

COMFORTWEIGH received FDA 510(k) clearance on 1987-06-24, under 510(k) number K871771.

Who is the listed applicant for COMFORTWEIGH?

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

What is the FDA product code for COMFORTWEIGH?

The FDA product code for COMFORTWEIGH is FRW.

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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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