MEDLINE MEDCREST SURGICAL GOWNS AND SURGICAL DRAPES
K-Number: K982694 · 1998-12-14
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Device Summary
Frequently Asked Questions
What is the MEDLINE MEDCREST SURGICAL GOWNS AND SURGICAL DRAPES?
MEDLINE MEDCREST SURGICAL GOWNS AND SURGICAL DRAPES is a medical device that received FDA 510(k) clearance on 1998-12-14. The listed applicant is Medline Industries, Inc.. The 510(k) number is K982694.
When did MEDLINE MEDCREST SURGICAL GOWNS AND SURGICAL DRAPES receive FDA 510(k) clearance?
MEDLINE MEDCREST SURGICAL GOWNS AND SURGICAL DRAPES received FDA 510(k) clearance on 1998-12-14, under 510(k) number K982694.
Who is the listed applicant for MEDLINE MEDCREST SURGICAL GOWNS AND SURGICAL DRAPES?
The FDA 510(k) record lists Medline Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDLINE MEDCREST SURGICAL GOWNS AND SURGICAL DRAPES?
The FDA product code for MEDLINE MEDCREST SURGICAL GOWNS AND SURGICAL DRAPES is FYA.
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 Medline Industries, 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: FYA)
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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