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FDA 510(k)

TASSI MK2

K-Number: K884835 · 1988-12-07

ApplicantTherapy Air Support Systems, Inc.
Decision Date1988-12-07
Product CodeINX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TASSI MK2 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 1988-12-07 under 510(k) number K884835. The device is classified under product code INX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TASSI MK2?

TASSI MK2 is a medical device that received FDA 510(k) clearance on 1988-12-07. The listed applicant is Therapy Air Support Systems, Inc.. The 510(k) number is K884835.

When did TASSI MK2 receive FDA 510(k) clearance?

TASSI MK2 received FDA 510(k) clearance on 1988-12-07, under 510(k) number K884835.

Who is the listed applicant for TASSI MK2?

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 MK2?

The FDA product code for TASSI MK2 is INX.

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.

K910851TASSI MK3 (TURNAIR)

Related Devices (Code: INX)

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.

K972176HOME CARE BEAD BEDKinetic Concepts, Inc.K964223CLINITRON RITE-HITEHill-Rom, Inc.K943385CLINITRON ELEXISSsi Medical Services, Inc.K942184CLINITRON AT HOME AIR FLUIDED THERAPYSsi Medical Services, Inc.K931168X-20 AIR SUPPORT BEDAmerican Life Support Technology, Inc.K934689LOW AIR LOSS MATTRESS, MODIFICATIONCardio Systems, 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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