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FDA 510(k)

JBAIDS Q FEVER DETECTION KIT

K-Number: K103207 · 2011-05-20

ApplicantIdaho Technology, Inc.
Decision Date2011-05-20
Product CodeOVF
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

JBAIDS Q FEVER DETECTION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Idaho Technology, Inc.. It received FDA 510(k) clearance on 2011-05-20 under 510(k) number K103207. The device is classified under product code OVF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JBAIDS Q FEVER DETECTION KIT?

JBAIDS Q FEVER DETECTION KIT is a medical device that received FDA 510(k) clearance on 2011-05-20. The listed applicant is Idaho Technology, Inc.. The 510(k) number is K103207.

When did JBAIDS Q FEVER DETECTION KIT receive FDA 510(k) clearance?

JBAIDS Q FEVER DETECTION KIT received FDA 510(k) clearance on 2011-05-20, under 510(k) number K103207.

Who is the listed applicant for JBAIDS Q FEVER DETECTION KIT?

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

What is the FDA product code for JBAIDS Q FEVER DETECTION KIT?

The FDA product code for JBAIDS Q FEVER DETECTION KIT is OVF.

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Other records listing Idaho Technology, 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.

K120267FILMARRAY RP PANELK110764FILMARRAY RP PANELK103175FILMARRAY RESPIRATORY PANEL (RP)K072631JBAIDS PLAQUE DETECTION KIT, MODEL JRPD-ASY-0123K072547JBAIDS TULAREMIA DETECTION KIT, MODEL JRPD-ASY-0124K071188MODIFICATION TO JBAIDS ANTHRAX DETECTION SYSTEM

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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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