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FDA 510(k)

TASSI MK3 (TURNAIR)

K-Number: K910851 · 1991-05-15

ApplicantTherapy Air Support Systems, Inc.
Decision Date1991-05-15
Product CodeIOQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TASSI MK3 (TURNAIR) is the device name listed in this FDA 510(k) record. The listed applicant is Therapy Air Support Systems, Inc.. It received FDA 510(k) clearance on 1991-05-15 under 510(k) number K910851. 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 TASSI MK3 (TURNAIR)?

TASSI MK3 (TURNAIR) is a medical device that received FDA 510(k) clearance on 1991-05-15. The listed applicant is Therapy Air Support Systems, Inc.. The 510(k) number is K910851.

When did TASSI MK3 (TURNAIR) receive FDA 510(k) clearance?

TASSI MK3 (TURNAIR) received FDA 510(k) clearance on 1991-05-15, under 510(k) number K910851.

Who is the listed applicant for TASSI MK3 (TURNAIR)?

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

What is the FDA product code for TASSI MK3 (TURNAIR)?

The FDA product code for TASSI MK3 (TURNAIR) 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.

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 Therapy Air Support Systems, 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.

K884835TASSI MK2

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 ProductsK970363HYDROTEC LOW AIR LOSS THERAPY BEDApex Metal, Inc.K970364AIRTEC2 LOW AIR LOSS THERAPY BEDApex Metal, Inc.K970636TOTALCARE., MODULAR THERAPY SYSTEM (MTS)Hill-Rom, Inc.K964873SILKAIR LOW AIRLOSS THERAPYHill-Rom, 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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