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FDA 510(k)

MEDPRO FLOTATION SYSTEM

K-Number: K771824 · 1977-10-19

ApplicantMedpro, Inc.
Decision Date1977-10-19
Product CodeIKY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDPRO FLOTATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medpro, Inc.. It received FDA 510(k) clearance on 1977-10-19 under 510(k) number K771824. The device is classified under product code IKY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDPRO FLOTATION SYSTEM?

MEDPRO FLOTATION SYSTEM is a medical device that received FDA 510(k) clearance on 1977-10-19. The listed applicant is Medpro, Inc.. The 510(k) number is K771824.

When did MEDPRO FLOTATION SYSTEM receive FDA 510(k) clearance?

MEDPRO FLOTATION SYSTEM received FDA 510(k) clearance on 1977-10-19, under 510(k) number K771824.

Who is the listed applicant for MEDPRO FLOTATION SYSTEM?

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

What is the FDA product code for MEDPRO FLOTATION SYSTEM?

The FDA product code for MEDPRO FLOTATION SYSTEM is IKY.

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 Medpro, 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.

K772062NEONATAL FLOTATION SYSTEMK760870HEEL/ELBOW FLOTATION CUSHIONK760613FLOTATION UNIT, CHAIR

Related Devices (Code: IKY)

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.

K914921SCM-3 AND ACCESSORIESGaymar Industries, Inc.K813226GEL FLOTATION MATTRESSJefferson Industries, Inc.K802833TETRA NATAL-MAT WATER FLOTATION MAT.Tetra Group U.S.A., Inc.K802781BEDDING PADS EGGCREATE PADSLeemart Bedding Mfg. Co.K780779ECONO-FLOAT WATER FLOTATION MATTRESSJefferson Industries, Inc.K772062NEONATAL FLOTATION SYSTEMMedpro, Inc.

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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