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FDA 510(k)

FAIRBANKS BABY SCALE

K-Number: K920812 · 1992-05-13

Decision Date1992-05-13
Product CodeFRW
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FAIRBANKS BABY SCALE is the device name listed in this FDA 510(k) record. The listed applicant is Fairbanks Scales, Inc.. It received FDA 510(k) clearance on 1992-05-13 under 510(k) number K920812. 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 FAIRBANKS BABY SCALE?

FAIRBANKS BABY SCALE is a medical device that received FDA 510(k) clearance on 1992-05-13. The listed applicant is Fairbanks Scales, Inc.. The 510(k) number is K920812.

When did FAIRBANKS BABY SCALE receive FDA 510(k) clearance?

FAIRBANKS BABY SCALE received FDA 510(k) clearance on 1992-05-13, under 510(k) number K920812.

Who is the listed applicant for FAIRBANKS BABY SCALE?

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

What is the FDA product code for FAIRBANKS BABY SCALE?

The FDA product code for FAIRBANKS BABY SCALE is FRW.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: FRW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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