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FDA 510(k)

NOVA PILLOW

K-Number: K895477 · 1990-01-10

ApplicantNova Health Systems, Inc.
Decision Date1990-01-10
Product CodeIQK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NOVA PILLOW is the device name listed in this FDA 510(k) record. The listed applicant is Nova Health Systems, Inc.. It received FDA 510(k) clearance on 1990-01-10 under 510(k) number K895477. The device is classified under product code IQK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVA PILLOW?

NOVA PILLOW is a medical device that received FDA 510(k) clearance on 1990-01-10. The listed applicant is Nova Health Systems, Inc.. The 510(k) number is K895477.

When did NOVA PILLOW receive FDA 510(k) clearance?

NOVA PILLOW received FDA 510(k) clearance on 1990-01-10, under 510(k) number K895477.

Who is the listed applicant for NOVA PILLOW?

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

What is the FDA product code for NOVA PILLOW?

The FDA product code for NOVA PILLOW is IQK.

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 Nova Health 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.

K893713NOVA OXYGEN TENTK780502NOVA AIR FLOATATION SYSTEM

Related Devices (Code: IQK)

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.

K930730DORMIE NECK SUPPORT SYSTEMThe Western Diagnostics Co.K926291SCHUL-TEC IMMOBILIZERMedical Emergency Support EquipmentK896042MEDICAL DISPOSABLE BEDDINGKeystone Veterinary Supplies, Inc.K882264BATTLE CREEK PILLOWBattle Creek Equipment Co.K850465CERVICAL COLLARS & HEAD HALTERSAbco Dealers, Inc.K832990STIFNICK IMMOBILIZING COLLARLaerdal California, 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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