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FDA 510(k)

CLEANTECH SYSTEM

K-Number: K882539 · 1988-08-08

ApplicantSchiff & Co.
Decision Date1988-08-08
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CLEANTECH SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Schiff & Co.. It received FDA 510(k) clearance on 1988-08-08 under 510(k) number K882539. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEANTECH SYSTEM?

CLEANTECH SYSTEM is a medical device that received FDA 510(k) clearance on 1988-08-08. The listed applicant is Schiff & Co.. The 510(k) number is K882539.

When did CLEANTECH SYSTEM receive FDA 510(k) clearance?

CLEANTECH SYSTEM received FDA 510(k) clearance on 1988-08-08, under 510(k) number K882539.

Who is the listed applicant for CLEANTECH SYSTEM?

The FDA 510(k) record lists Schiff & Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLEANTECH SYSTEM?

The FDA product code for CLEANTECH SYSTEM is JKA.

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Related Devices (Code: JKA)

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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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