FAST WRAP #M 101
K-Number: K891215 · 1989-04-14
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Device Summary
Frequently Asked Questions
What is the FAST WRAP #M 101?
FAST WRAP #M 101 is a medical device that received FDA 510(k) clearance on 1989-04-14. The listed applicant is Pro-Safe Professional Linens, Inc.. The 510(k) number is K891215.
When did FAST WRAP #M 101 receive FDA 510(k) clearance?
FAST WRAP #M 101 received FDA 510(k) clearance on 1989-04-14, under 510(k) number K891215.
Who is the listed applicant for FAST WRAP #M 101?
The FDA 510(k) record lists Pro-Safe Professional Linens, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FAST WRAP #M 101?
The FDA product code for FAST WRAP #M 101 is KCT.
Other records listing Pro-Safe Professional Linens, 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: KCT)
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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