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FDA 510(k)

IDA RAPID O2A SYSTEM

K-Number: K820483 · 1982-03-15

ApplicantInnovative Diagnostic Systems, Inc.
Decision Date1982-03-15
Product CodeJSP
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

IDA RAPID O2A 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 1982-03-15 under 510(k) number K820483. The device is classified under product code JSP. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IDA RAPID O2A SYSTEM?

IDA RAPID O2A SYSTEM is a medical device that received FDA 510(k) clearance on 1982-03-15. The listed applicant is Innovative Diagnostic Systems, Inc.. The 510(k) number is K820483.

When did IDA RAPID O2A SYSTEM receive FDA 510(k) clearance?

IDA RAPID O2A SYSTEM received FDA 510(k) clearance on 1982-03-15, under 510(k) number K820483.

Who is the listed applicant for IDA RAPID O2A 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 IDA RAPID O2A SYSTEM?

The FDA product code for IDA RAPID O2A SYSTEM is JSP.

Related Clinical Trials

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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 SYSTEMK900517RAPID NF SYSTEMK882960IDS RAPID ANA SYSTEMK881501MODIFIED IDS RAPID NH SYSTEMK852871IDS RAPID SS/U SYSTEM

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Related Devices (Code: JSP)

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.

K945489LYFO(TM) DIFFERENTIAL DISKMicrobiologics, Inc.K945487LYFO(TM) DIFFERENTIAL DISKMicrobiologics, Inc.K945488LYFO(TM) DIFFERENTIAL DISKMicrobiologics, Inc.K944528BBLCRYSTAL ANAEROBE ID SYSTEMBecton Dickinson Microbiology SystemsK910666VITEK ANAEROBE IDENTIFICATION CARD, MODIFICATIONVitek Systems, Inc.K900996VITEK ANAEROBE IDENTIFICATION CARDVitek 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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