CARETEX OR TOWEL
K-Number: K884112 · 1988-10-13
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Device Summary
Frequently Asked Questions
What is the CARETEX OR TOWEL?
CARETEX OR TOWEL is a medical device that received FDA 510(k) clearance on 1988-10-13. The listed applicant is James River Corp.. The 510(k) number is K884112.
When did CARETEX OR TOWEL receive FDA 510(k) clearance?
CARETEX OR TOWEL received FDA 510(k) clearance on 1988-10-13, under 510(k) number K884112.
Who is the listed applicant for CARETEX OR TOWEL?
The FDA 510(k) record lists James River Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CARETEX OR TOWEL?
The FDA product code for CARETEX OR TOWEL is KKX.
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 James River Corp. 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: KKX)
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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