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FDA 510(k)

DIGITAL BABY SCALE MODEL BLB-12

K-Number: K932572 · 1993-11-16

Decision Date1993-11-16
Product CodeFRW
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DIGITAL BABY SCALE MODEL BLB-12 is the device name listed in this FDA 510(k) record. The listed applicant is Tanita Corp. of America. It received FDA 510(k) clearance on 1993-11-16 under 510(k) number K932572. 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 DIGITAL BABY SCALE MODEL BLB-12?

DIGITAL BABY SCALE MODEL BLB-12 is a medical device that received FDA 510(k) clearance on 1993-11-16. The listed applicant is Tanita Corp. of America. The 510(k) number is K932572.

When did DIGITAL BABY SCALE MODEL BLB-12 receive FDA 510(k) clearance?

DIGITAL BABY SCALE MODEL BLB-12 received FDA 510(k) clearance on 1993-11-16, under 510(k) number K932572.

Who is the listed applicant for DIGITAL BABY SCALE MODEL BLB-12?

The FDA 510(k) record lists Tanita Corp. of America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIGITAL BABY SCALE MODEL BLB-12?

The FDA product code for DIGITAL BABY SCALE MODEL BLB-12 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.

Other records listing Tanita Corp. of America as applicant

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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