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FDA 510(k)

APOLLO MOBILE SCALE

K-Number: K905061 · 1991-02-12

ApplicantApollo Enterprise, Ltd. Co.
Decision Date1991-02-12
Product CodeFRW
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

APOLLO MOBILE SCALE is the device name listed in this FDA 510(k) record. The listed applicant is Apollo Enterprise, Ltd. Co.. It received FDA 510(k) clearance on 1991-02-12 under 510(k) number K905061. 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 APOLLO MOBILE SCALE?

APOLLO MOBILE SCALE is a medical device that received FDA 510(k) clearance on 1991-02-12. The listed applicant is Apollo Enterprise, Ltd. Co.. The 510(k) number is K905061.

When did APOLLO MOBILE SCALE receive FDA 510(k) clearance?

APOLLO MOBILE SCALE received FDA 510(k) clearance on 1991-02-12, under 510(k) number K905061.

Who is the listed applicant for APOLLO MOBILE SCALE?

The FDA 510(k) record lists Apollo Enterprise, Ltd. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for APOLLO MOBILE SCALE?

The FDA product code for APOLLO MOBILE SCALE 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 Apollo Enterprise, Ltd. 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.

K905122SENTRY SCALEK874236APOLLO CONDOM

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.K955177OLYMPIC SMART SCALEOlympic Medical Corp.K954846OLYMPIC 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.

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