DISPOSABLE PATIENT BLANKET
K-Number: K843038 · 1984-10-24
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Device Summary
Frequently Asked Questions
What is the DISPOSABLE PATIENT BLANKET?
DISPOSABLE PATIENT BLANKET is a medical device that received FDA 510(k) clearance on 1984-10-24. The listed applicant is Anago, Inc.. The 510(k) number is K843038.
When did DISPOSABLE PATIENT BLANKET receive FDA 510(k) clearance?
DISPOSABLE PATIENT BLANKET received FDA 510(k) clearance on 1984-10-24, under 510(k) number K843038.
Who is the listed applicant for DISPOSABLE PATIENT BLANKET?
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 PATIENT BLANKET?
The FDA product code for DISPOSABLE PATIENT BLANKET 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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