LASER RESISTANT DRAPE
K-Number: K873141 · 1987-10-23
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Device Summary
Frequently Asked Questions
What is the LASER RESISTANT DRAPE?
LASER RESISTANT DRAPE is a medical device that received FDA 510(k) clearance on 1987-10-23. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K873141.
When did LASER RESISTANT DRAPE receive FDA 510(k) clearance?
LASER RESISTANT DRAPE received FDA 510(k) clearance on 1987-10-23, under 510(k) number K873141.
Who is the listed applicant for LASER RESISTANT DRAPE?
The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LASER RESISTANT DRAPE?
The FDA product code for LASER RESISTANT DRAPE 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 Baxter Healthcare 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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