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)

ACME MODEL 8500 WHEELCHAIR SCALE

K-Number: K910055 · 1991-01-14

Decision Date1991-01-14
Product CodeINF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ACME MODEL 8500 WHEELCHAIR SCALE is the device name listed in this FDA 510(k) record. The listed applicant is Acme Medical Scale Co.. It received FDA 510(k) clearance on 1991-01-14 under 510(k) number K910055. The device is classified under product code INF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACME MODEL 8500 WHEELCHAIR SCALE?

ACME MODEL 8500 WHEELCHAIR SCALE is a medical device that received FDA 510(k) clearance on 1991-01-14. The listed applicant is Acme Medical Scale Co.. The 510(k) number is K910055.

When did ACME MODEL 8500 WHEELCHAIR SCALE receive FDA 510(k) clearance?

ACME MODEL 8500 WHEELCHAIR SCALE received FDA 510(k) clearance on 1991-01-14, under 510(k) number K910055.

Who is the listed applicant for ACME MODEL 8500 WHEELCHAIR SCALE?

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 ACME MODEL 8500 WHEELCHAIR SCALE?

The FDA product code for ACME MODEL 8500 WHEELCHAIR SCALE is INF.

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.

View all 10 devices →

Related Devices (Code: INF)

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.

↑