RECEIVING BLANKET
K-Number: K904274 · 1990-10-26
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Device Summary
Frequently Asked Questions
What is the RECEIVING BLANKET?
RECEIVING BLANKET is a medical device that received FDA 510(k) clearance on 1990-10-26. The listed applicant is Anago, Inc.. The 510(k) number is K904274.
When did RECEIVING BLANKET receive FDA 510(k) clearance?
RECEIVING BLANKET received FDA 510(k) clearance on 1990-10-26, under 510(k) number K904274.
Who is the listed applicant for RECEIVING 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 RECEIVING BLANKET?
The FDA product code for RECEIVING 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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