CERVICAL PILLOW
K-Number: K830350 · 1983-03-09
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Device Summary
Frequently Asked Questions
What is the CERVICAL PILLOW?
CERVICAL PILLOW is a medical device that received FDA 510(k) clearance on 1983-03-09. The listed applicant is Deip Enterprises, Inc.. The 510(k) number is K830350.
When did CERVICAL PILLOW receive FDA 510(k) clearance?
CERVICAL PILLOW received FDA 510(k) clearance on 1983-03-09, under 510(k) number K830350.
Who is the listed applicant for CERVICAL PILLOW?
The FDA 510(k) record lists Deip Enterprises, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CERVICAL PILLOW?
The FDA product code for CERVICAL 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.
Other records listing Deip Enterprises, 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.
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.
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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