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FDA 510(k)

WECK CONCENTRATED LIQUID CLEANER

K-Number: K861587 · 1986-05-19

ApplicantPalmetto Chemical & Supply Co., Inc.
Decision Date1986-05-19
Product CodeFLG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

WECK CONCENTRATED LIQUID CLEANER 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 1986-05-19 under 510(k) number K861587. The device is classified under product code FLG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WECK CONCENTRATED LIQUID CLEANER?

WECK CONCENTRATED LIQUID CLEANER is a medical device that received FDA 510(k) clearance on 1986-05-19. The listed applicant is Palmetto Chemical & Supply Co., Inc.. The 510(k) number is K861587.

When did WECK CONCENTRATED LIQUID CLEANER receive FDA 510(k) clearance?

WECK CONCENTRATED LIQUID CLEANER received FDA 510(k) clearance on 1986-05-19, under 510(k) number K861587.

Who is the listed applicant for WECK CONCENTRATED LIQUID CLEANER?

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 WECK CONCENTRATED LIQUID CLEANER?

The FDA product code for WECK CONCENTRATED LIQUID CLEANER 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.

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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. 850-155K861591WECK-LUBE, CATALOG NO. 850-150

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.

K944950KLENZYMECalgon Corp.K944494ALSA-KLENZCalgon Vestal Div.K944033BILL EVANS-KLENZCalgon Vestal Div.K940263NPH-KLENZCalgon Corp.K941163MON-KLENZCalgon Vestal Div.K935063INSTRU KLENZCalgon Corp.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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