DIGITAL BEDSIDE SCALE #5000
K-Number: K830171 · 1983-02-18
Advertisement
Device Summary
Frequently Asked Questions
What is the DIGITAL BEDSIDE SCALE #5000?
DIGITAL BEDSIDE SCALE #5000 is a medical device that received FDA 510(k) clearance on 1983-02-18. The listed applicant is Acme Medical Scale Co.. The 510(k) number is K830171.
When did DIGITAL BEDSIDE SCALE #5000 receive FDA 510(k) clearance?
DIGITAL BEDSIDE SCALE #5000 received FDA 510(k) clearance on 1983-02-18, under 510(k) number K830171.
Who is the listed applicant for DIGITAL BEDSIDE SCALE #5000?
The FDA 510(k) record lists Acme Medical Scale Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIGITAL BEDSIDE SCALE #5000?
The FDA product code for DIGITAL BEDSIDE SCALE #5000 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 Acme Medical Scale Co. 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.
Advertisement