DISPOSABLE PILLOW
K-Number: K810264 · 1981-02-09
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Device Summary
Frequently Asked Questions
What is the DISPOSABLE PILLOW?
DISPOSABLE PILLOW is a medical device that received FDA 510(k) clearance on 1981-02-09. The listed applicant is Anago, Inc.. The 510(k) number is K810264.
When did DISPOSABLE PILLOW receive FDA 510(k) clearance?
DISPOSABLE PILLOW received FDA 510(k) clearance on 1981-02-09, under 510(k) number K810264.
Who is the listed applicant for DISPOSABLE PILLOW?
The FDA 510(k) record lists Anago, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISPOSABLE PILLOW?
The FDA product code for DISPOSABLE PILLOW is KME.
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 Anago, 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: KME)
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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