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FDA 510(k)

WECK-LUBE, CATALOG NO. 850-150

K-Number: K861591 · 1986-05-23

ApplicantPalmetto Chemical & Supply Co., Inc.
Decision Date1986-05-23
Product Code
DecisionSubstantially Equivalent

Device Summary

WECK-LUBE, CATALOG NO. 850-150 is the device name listed in this FDA 510(k) record. The listed applicant is Palmetto Chemical & Supply Co., Inc.. It received FDA 510(k) clearance on 1986-05-23 under 510(k) number K861591. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WECK-LUBE, CATALOG NO. 850-150?

WECK-LUBE, CATALOG NO. 850-150 is a medical device that received FDA 510(k) clearance on 1986-05-23. The listed applicant is Palmetto Chemical & Supply Co., Inc.. The 510(k) number is K861591.

When did WECK-LUBE, CATALOG NO. 850-150 receive FDA 510(k) clearance?

WECK-LUBE, CATALOG NO. 850-150 received FDA 510(k) clearance on 1986-05-23, under 510(k) number K861591.

Who is the listed applicant for WECK-LUBE, CATALOG NO. 850-150?

The FDA 510(k) record lists Palmetto Chemical & Supply Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

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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.

K861590WEC-KLEEN, CATALOG N. 850-102K861592WEC-WASH, CATALOG NO. 850-115K861588WECK INSTRUMENT CLEANER, CAT. NO. 850-103K861589WECK-KREEM, CATALOG NO. 850-155K861587WECK CONCENTRATED LIQUID CLEANER

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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