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FDA 510(k)

FLOTATION UNIT, CHAIR

K-Number: K760613 · 1976-10-14

ApplicantMedpro, Inc.
Decision Date1976-10-14
Product CodeKIC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FLOTATION UNIT, CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Medpro, Inc.. It received FDA 510(k) clearance on 1976-10-14 under 510(k) number K760613. The device is classified under product code KIC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLOTATION UNIT, CHAIR?

FLOTATION UNIT, CHAIR is a medical device that received FDA 510(k) clearance on 1976-10-14. The listed applicant is Medpro, Inc.. The 510(k) number is K760613.

When did FLOTATION UNIT, CHAIR receive FDA 510(k) clearance?

FLOTATION UNIT, CHAIR received FDA 510(k) clearance on 1976-10-14, under 510(k) number K760613.

Who is the listed applicant for FLOTATION UNIT, CHAIR?

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 FLOTATION UNIT, CHAIR?

The FDA product code for FLOTATION UNIT, CHAIR is KIC.

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.

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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 SYSTEMK771824MEDPRO FLOTATION SYSTEMK760870HEEL/ELBOW FLOTATION CUSHION

Related Devices (Code: KIC)

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.

K960189GEL-T CUSHIONSpan-America Medical Systems, Inc.K953352PROTEAM CUSHIONIskra.MedK954117CUSTOMCARE SEATING SYSTEMSpan-America Medical Systems, Inc.K950085MULTICURE(R) S GEL PADMultigestion (Deutschland) GmbHK945667MICOS MICROPULSE(TM) ALTERNATING PRESSURE WHEELCHAIR CUSHIONMicos Medical SystemsK941858GEL CUSHIONHollister, 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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