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FDA 510(k)

RAPIDEC COLI

K-Number: K890626 · 1989-06-02

ApplicantDms Products, Inc.
Decision Date1989-06-02
Product CodeJSS
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

RAPIDEC COLI is the device name listed in this FDA 510(k) record. The listed applicant is Dms Products, Inc.. It received FDA 510(k) clearance on 1989-06-02 under 510(k) number K890626. The device is classified under product code JSS. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAPIDEC COLI?

RAPIDEC COLI is a medical device that received FDA 510(k) clearance on 1989-06-02. The listed applicant is Dms Products, Inc.. The 510(k) number is K890626.

When did RAPIDEC COLI receive FDA 510(k) clearance?

RAPIDEC COLI received FDA 510(k) clearance on 1989-06-02, under 510(k) number K890626.

Who is the listed applicant for RAPIDEC COLI?

The FDA 510(k) record lists Dms Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RAPIDEC COLI?

The FDA product code for RAPIDEC COLI is JSS.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Dms Products, 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.

K891004RAPIDEC STAPHK894805RAPIDEC URK890625JAMES REAGENTK854733API 20 EC (ENTEROBACTERIACEAE)(IDENTIFICATION KIT)K854732API 50 CHB (CULTURE MEDIA)

Related Devices (Code: JSS)

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.

K123418GRAM-NEGATIVE QUICKFISH BCAdvandx, Inc.K101558GNR TRAFFIC LIGHT PNA FISHAdvandx, Inc.K092236E.COLI/P. AERUGINOSA PNA FISHAdvandx, Inc.K092393EK/P. AERUGINOSA PNA FISHAdvandx, Inc.K082068E. COLI PNA FISHAdvandx, Inc.K081433EK/P. AERUGINOSA PNA FISHAdvandx, Inc.

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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