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)

SCALE, ACME DIGITAL BEDSIDE

K-Number: K781832 · 1978-12-07

ApplicantAcme Medical Scale Co.
Decision Date1978-12-07
Product CodeFRW
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SCALE, ACME DIGITAL BEDSIDE 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 1978-12-07 under 510(k) number K781832. 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 SCALE, ACME DIGITAL BEDSIDE?

SCALE, ACME DIGITAL BEDSIDE is a medical device that received FDA 510(k) clearance on 1978-12-07. The listed applicant is Acme Medical Scale Co.. The 510(k) number is K781832.

When did SCALE, ACME DIGITAL BEDSIDE receive FDA 510(k) clearance?

SCALE, ACME DIGITAL BEDSIDE received FDA 510(k) clearance on 1978-12-07, under 510(k) number K781832.

Who is the listed applicant for SCALE, ACME DIGITAL BEDSIDE?

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 SCALE, ACME DIGITAL BEDSIDE?

The FDA product code for SCALE, ACME DIGITAL BEDSIDE 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K926174MODEL 9100 H.R. INFANT SCALEK922119MODEL 5002 LIFT WEIGH-SCALEK910055ACME MODEL 8500 WHEELCHAIR SCALEK852278ACME(BRAND) LOW-PROFILE WHEELCHAIR SCALE, 17400K851014ACME LOW-PROFILE CHAIR SCAL 7300K841534ACME DIGITAL INFANT SCALE-30

View all 10 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.

K955357OLYMPIC SMART SCALE MODEL 50/50RAOlympic Medical Corp.K954846OLYMPIC SMART SCALEOlympic Medical Corp.K955177OLYMPIC SMART SCALEOlympic Medical Corp.K952649WARM-SCALEOlympic Medical Corp.K943587ADVANCED IN-BED WEIGH SYSTEMFuture Systems, Inc.K932572DIGITAL BABY SCALE MODEL BLB-12Tanita Corp. of America

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.

↑