VAAKA BABY SCALE
K-Number: K902545 · 1990-07-26
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Device Summary
Frequently Asked Questions
What is the VAAKA BABY SCALE?
VAAKA BABY SCALE is a medical device that received FDA 510(k) clearance on 1990-07-26. The listed applicant is Ferguson Medical. The 510(k) number is K902545.
When did VAAKA BABY SCALE receive FDA 510(k) clearance?
VAAKA BABY SCALE received FDA 510(k) clearance on 1990-07-26, under 510(k) number K902545.
Who is the listed applicant for VAAKA BABY SCALE?
The FDA 510(k) record lists Ferguson Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VAAKA BABY SCALE?
The FDA product code for VAAKA 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.
Other records listing Ferguson Medical 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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