MEDIFIX GRADUATED SCALE
K-Number: K813195 · 1981-12-29
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Device Summary
Frequently Asked Questions
What is the MEDIFIX GRADUATED SCALE?
MEDIFIX GRADUATED SCALE is a medical device that received FDA 510(k) clearance on 1981-12-29. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K813195.
When did MEDIFIX GRADUATED SCALE receive FDA 510(k) clearance?
MEDIFIX GRADUATED SCALE received FDA 510(k) clearance on 1981-12-29, under 510(k) number K813195.
Who is the listed applicant for MEDIFIX GRADUATED SCALE?
The FDA 510(k) record lists Burron Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDIFIX GRADUATED SCALE?
The FDA product code for MEDIFIX GRADUATED SCALE is KRK.
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 Burron Medical Products, Inc. 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: KRK)
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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