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FDA 510(k)

SERIM RESIDUAL CHLORINE TEST KIT

K-Number: K901734 · 1990-09-13

Decision Date1990-09-13
Product CodeFKJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SERIM RESIDUAL CHLORINE TEST KIT is the device name listed in this FDA 510(k) record. The listed applicant is Serim Research Corp.. It received FDA 510(k) clearance on 1990-09-13 under 510(k) number K901734. The device is classified under product code FKJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERIM RESIDUAL CHLORINE TEST KIT?

SERIM RESIDUAL CHLORINE TEST KIT is a medical device that received FDA 510(k) clearance on 1990-09-13. The listed applicant is Serim Research Corp.. The 510(k) number is K901734.

When did SERIM RESIDUAL CHLORINE TEST KIT receive FDA 510(k) clearance?

SERIM RESIDUAL CHLORINE TEST KIT received FDA 510(k) clearance on 1990-09-13, under 510(k) number K901734.

Who is the listed applicant for SERIM RESIDUAL CHLORINE TEST KIT?

The FDA 510(k) record lists Serim Research Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SERIM RESIDUAL CHLORINE TEST KIT?

The FDA product code for SERIM RESIDUAL CHLORINE TEST KIT is FKJ.

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 Serim Research 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.

View all 27 devices →

Related Devices (Code: FKJ)

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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