WEC-KLEEN, CATALOG N. 850-102
K-Number: K861590 · 1986-06-17
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Device Summary
Frequently Asked Questions
What is the WEC-KLEEN, CATALOG N. 850-102?
WEC-KLEEN, CATALOG N. 850-102 is a medical device that received FDA 510(k) clearance on 1986-06-17. The listed applicant is Palmetto Chemical & Supply Co., Inc.. The 510(k) number is K861590.
When did WEC-KLEEN, CATALOG N. 850-102 receive FDA 510(k) clearance?
WEC-KLEEN, CATALOG N. 850-102 received FDA 510(k) clearance on 1986-06-17, under 510(k) number K861590.
Who is the listed applicant for WEC-KLEEN, CATALOG N. 850-102?
The FDA 510(k) record lists Palmetto Chemical & Supply Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WEC-KLEEN, CATALOG N. 850-102?
The FDA product code for WEC-KLEEN, CATALOG N. 850-102 is FLG.
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 Palmetto Chemical & Supply Co., 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: FLG)
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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