Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

OLYMPIC SMART SCALE MODEL 50/50RA

K-Number: K955357 · 1996-01-30

Decision Date1996-01-30
Product CodeFRW
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

OLYMPIC SMART SCALE MODEL 50/50RA is the device name listed in this FDA 510(k) record. The listed applicant is Olympic Medical Corp.. It received FDA 510(k) clearance on 1996-01-30 under 510(k) number K955357. 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 OLYMPIC SMART SCALE MODEL 50/50RA?

OLYMPIC SMART SCALE MODEL 50/50RA is a medical device that received FDA 510(k) clearance on 1996-01-30. The listed applicant is Olympic Medical Corp.. The 510(k) number is K955357.

When did OLYMPIC SMART SCALE MODEL 50/50RA receive FDA 510(k) clearance?

OLYMPIC SMART SCALE MODEL 50/50RA received FDA 510(k) clearance on 1996-01-30, under 510(k) number K955357.

Who is the listed applicant for OLYMPIC SMART SCALE MODEL 50/50RA?

The FDA 510(k) record lists Olympic Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OLYMPIC SMART SCALE MODEL 50/50RA?

The FDA product code for OLYMPIC SMART SCALE MODEL 50/50RA 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 Olympic Medical Corp. 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.

View all 37 devices →

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.

↑