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FDA 510(k)

POWER PILLOW

K-Number: K923805 · 1993-02-12

ApplicantNova Teknic, Inc.
Decision Date1993-02-12
Product CodeBXB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

POWER PILLOW is the device name listed in this FDA 510(k) record. The listed applicant is Nova Teknic, Inc.. It received FDA 510(k) clearance on 1993-02-12 under 510(k) number K923805. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWER PILLOW?

POWER PILLOW is a medical device that received FDA 510(k) clearance on 1993-02-12. The listed applicant is Nova Teknic, Inc.. The 510(k) number is K923805.

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

POWER PILLOW received FDA 510(k) clearance on 1993-02-12, under 510(k) number K923805.

Who is the listed applicant for POWER PILLOW?

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

What is the FDA product code for POWER PILLOW?

The FDA product code for POWER PILLOW is BXB.

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Related Devices (Code: BXB)

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.

K072887G-TRAINER MEDICALAlter-G, Inc.K003272FLO-BOOTDiscovery Group, LLCK952975ANKLE CALF EXERCISER PHLEBOPUMPPrevent Products, Inc.K953456E-Z FLEXFluid Motion Biotechnologies, Inc.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.

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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