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FDA 510(k)

HAMILTON PEDIATRICS SCALE

K-Number: K833754 · 1984-01-11

ApplicantBefour, Inc.
Decision Date1984-01-11
Product CodeFRW
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HAMILTON PEDIATRICS SCALE is the device name listed in this FDA 510(k) record. The listed applicant is Befour, Inc.. It received FDA 510(k) clearance on 1984-01-11 under 510(k) number K833754. 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 HAMILTON PEDIATRICS SCALE?

HAMILTON PEDIATRICS SCALE is a medical device that received FDA 510(k) clearance on 1984-01-11. The listed applicant is Befour, Inc.. The 510(k) number is K833754.

When did HAMILTON PEDIATRICS SCALE receive FDA 510(k) clearance?

HAMILTON PEDIATRICS SCALE received FDA 510(k) clearance on 1984-01-11, under 510(k) number K833754.

Who is the listed applicant for HAMILTON PEDIATRICS SCALE?

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

What is the FDA product code for HAMILTON PEDIATRICS SCALE?

The FDA product code for HAMILTON PEDIATRICS SCALE is FRW.

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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.

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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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