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FDA 510(k)

BOMDAL TRAVELMASTER LIFT

K-Number: K862146 · 1986-07-15

ApplicantBomdal Medical Equipment, Inc.
Decision Date1986-07-15
Product CodeFNG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BOMDAL TRAVELMASTER LIFT is the device name listed in this FDA 510(k) record. The listed applicant is Bomdal Medical Equipment, Inc.. It received FDA 510(k) clearance on 1986-07-15 under 510(k) number K862146. The device is classified under product code FNG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOMDAL TRAVELMASTER LIFT?

BOMDAL TRAVELMASTER LIFT is a medical device that received FDA 510(k) clearance on 1986-07-15. The listed applicant is Bomdal Medical Equipment, Inc.. The 510(k) number is K862146.

When did BOMDAL TRAVELMASTER LIFT receive FDA 510(k) clearance?

BOMDAL TRAVELMASTER LIFT received FDA 510(k) clearance on 1986-07-15, under 510(k) number K862146.

Who is the listed applicant for BOMDAL TRAVELMASTER LIFT?

The FDA 510(k) record lists Bomdal Medical Equipment, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BOMDAL TRAVELMASTER LIFT?

The FDA product code for BOMDAL TRAVELMASTER LIFT is FNG.

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 Bomdal Medical Equipment, Inc. 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.

K862147BOMDAL STANDARD LIFT

Related Devices (Code: FNG)

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.

K121287HT-WEDGED.T. Davis Enterprises Ltd. T/A Hovertech Int'LK041503HOVERJACK AIR PATIENT LIFT DEVICED.T. Davis Enterprises , Ltd.K940872PATIENT SUPPORT SYSTEMArylift, Inc.K935351A.C. POWER PATIENT LIFTKen KemmererK926411SAF-LIFT/SAF-KARYArjo-Century, Inc.K912769PATIENT LIFT AND TRANSPORTCentury Manufacturing Co.

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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