Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SERIM PERACETIC ACID REAGENT STRIPS

K-Number: K910320 · 1991-05-01

Decision Date1991-05-01
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SERIM PERACETIC ACID REAGENT STRIPS 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 1991-05-01 under 510(k) number K910320. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERIM PERACETIC ACID REAGENT STRIPS?

SERIM PERACETIC ACID REAGENT STRIPS is a medical device that received FDA 510(k) clearance on 1991-05-01. The listed applicant is Serim Research Corp.. The 510(k) number is K910320.

When did SERIM PERACETIC ACID REAGENT STRIPS receive FDA 510(k) clearance?

SERIM PERACETIC ACID REAGENT STRIPS received FDA 510(k) clearance on 1991-05-01, under 510(k) number K910320.

Who is the listed applicant for SERIM PERACETIC ACID REAGENT STRIPS?

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 PERACETIC ACID REAGENT STRIPS?

The FDA product code for SERIM PERACETIC ACID REAGENT STRIPS is JOJ.

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: JOJ)

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.

↑