WELLS LAMONT CUT RESISTANT SURGICAL GLOVE LINERS
K-Number: K922407 · 1993-06-15
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Device Summary
Frequently Asked Questions
What is the WELLS LAMONT CUT RESISTANT SURGICAL GLOVE LINERS?
WELLS LAMONT CUT RESISTANT SURGICAL GLOVE LINERS is a medical device that received FDA 510(k) clearance on 1993-06-15. The listed applicant is Wells Lamont Corp.. The 510(k) number is K922407.
When did WELLS LAMONT CUT RESISTANT SURGICAL GLOVE LINERS receive FDA 510(k) clearance?
WELLS LAMONT CUT RESISTANT SURGICAL GLOVE LINERS received FDA 510(k) clearance on 1993-06-15, under 510(k) number K922407.
Who is the listed applicant for WELLS LAMONT CUT RESISTANT SURGICAL GLOVE LINERS?
The FDA 510(k) record lists Wells Lamont Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WELLS LAMONT CUT RESISTANT SURGICAL GLOVE LINERS?
The FDA product code for WELLS LAMONT CUT RESISTANT SURGICAL GLOVE LINERS is LYU.
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 Wells Lamont 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: LYU)
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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