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FDA 510(k)

RAPID NF SYSTEM

K-Number: K900517 · 1990-03-13

ApplicantInnovative Diagnostic Systems, Inc.
Decision Date1990-03-13
Product CodeJSW
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

RAPID NF SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Diagnostic Systems, Inc.. It received FDA 510(k) clearance on 1990-03-13 under 510(k) number K900517. The device is classified under product code JSW. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAPID NF SYSTEM?

RAPID NF SYSTEM is a medical device that received FDA 510(k) clearance on 1990-03-13. The listed applicant is Innovative Diagnostic Systems, Inc.. The 510(k) number is K900517.

When did RAPID NF SYSTEM receive FDA 510(k) clearance?

RAPID NF SYSTEM received FDA 510(k) clearance on 1990-03-13, under 510(k) number K900517.

Who is the listed applicant for RAPID NF SYSTEM?

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

What is the FDA product code for RAPID NF SYSTEM?

The FDA product code for RAPID NF SYSTEM is JSW.

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 Innovative Diagnostic Systems, 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.

K962966IDS RAPID CB PLUS SYSTEMK943621RAPID YEAST PLUS SYSTEMK882960IDS RAPID ANA SYSTEMK881501MODIFIED IDS RAPID NH SYSTEMK852871IDS RAPID SS/U SYSTEMK852110IDS RAPID E PLUS SYSTEM

View all 11 devices →

Related Devices (Code: JSW)

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.

K922768RAPID NFT, MODIFICATIONBiomerieux Vitek, Inc.K870769AUSTIN NONFERMENTER KITAustin Biological LaboratoriesK790992PSEUDO-PALETTE TMMicro-Palettes, Inc.K772112NON-FERMENTER SYSTEMCorning Medical & ScientificK770745PANEL, GNF, MICRO-IDMicro-Media Systems, 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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