DIGITAL BABY SCALE MODEL BLB-12
K-Number: K932572 · 1993-11-16
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Device Summary
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
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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