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FDA 510(k)

MEDSENTRY FLOTATION SYSTEM

K-Number: K863152 · 1986-09-23

ApplicantMedsentry Corp.
Decision Date1986-09-23
Product CodeFNM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDSENTRY FLOTATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medsentry Corp.. It received FDA 510(k) clearance on 1986-09-23 under 510(k) number K863152. The device is classified under product code FNM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDSENTRY FLOTATION SYSTEM?

MEDSENTRY FLOTATION SYSTEM is a medical device that received FDA 510(k) clearance on 1986-09-23. The listed applicant is Medsentry Corp.. The 510(k) number is K863152.

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

MEDSENTRY FLOTATION SYSTEM received FDA 510(k) clearance on 1986-09-23, under 510(k) number K863152.

Who is the listed applicant for MEDSENTRY FLOTATION SYSTEM?

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

What is the FDA product code for MEDSENTRY FLOTATION SYSTEM?

The FDA product code for MEDSENTRY FLOTATION SYSTEM is FNM.

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 Medsentry Corp. 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.

K844499MEDSENTRY SOFTOUCH SYSTEM

Related Devices (Code: FNM)

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.

K973169PRESSURE GUARD SITE SELECT (A)Span-America Medical Systems, Inc.K972022ZAK-2000Cardio Systems, Inc.K974319MIGHTY AIRWheelchairs of KansasK974070PHYSIO/1000Physio Designs, Inc.K972549SIMPULSEKinetic Concepts, Inc.K970081SUPER AIR 9000 ALTERNATING AIR FLOATATION MATTRESS SYSTEMCathay Consolidated, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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