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FDA 510(k)

TOTAL CONTACT SEAT RIPPLE SYSTEM

K-Number: K943433 · 1995-07-31

ApplicantNumotech, Inc.
Decision Date1995-07-31
Product CodeIOQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TOTAL CONTACT SEAT RIPPLE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Numotech, Inc.. It received FDA 510(k) clearance on 1995-07-31 under 510(k) number K943433. The device is classified under product code IOQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOTAL CONTACT SEAT RIPPLE SYSTEM?

TOTAL CONTACT SEAT RIPPLE SYSTEM is a medical device that received FDA 510(k) clearance on 1995-07-31. The listed applicant is Numotech, Inc.. The 510(k) number is K943433.

When did TOTAL CONTACT SEAT RIPPLE SYSTEM receive FDA 510(k) clearance?

TOTAL CONTACT SEAT RIPPLE SYSTEM received FDA 510(k) clearance on 1995-07-31, under 510(k) number K943433.

Who is the listed applicant for TOTAL CONTACT SEAT RIPPLE SYSTEM?

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

What is the FDA product code for TOTAL CONTACT SEAT RIPPLE SYSTEM?

The FDA product code for TOTAL CONTACT SEAT RIPPLE SYSTEM is IOQ.

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 Numotech, 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.

K981949NUMOBAG

Related Devices (Code: IOQ)

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.

K122473TOTALCARE SPOT TOTALCARE BARIATRIC TOTALCARE DUO TOATALCARE BED SYSTEM TOTALCARE DUO2Hill-RomK973624NURSE'S AID PATIENT ROTATION SYSTEMAir Med Assist ProductsK970364AIRTEC2 LOW AIR LOSS THERAPY BEDApex Metal, Inc.K970363HYDROTEC LOW AIR LOSS THERAPY BEDApex Metal, Inc.K970636TOTALCARE., MODULAR THERAPY SYSTEM (MTS)Hill-Rom, Inc.K964873SILKAIR LOW AIRLOSS THERAPYHill-Rom, 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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