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FDA 510(k)

JBAIDS TULAREMIA DETECTION KIT, MODEL JRPD-ASY-0124

K-Number: K072547 · 2007-12-19

ApplicantIdaho Technology, Inc.
Decision Date2007-12-19
Product CodeOEH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

JBAIDS TULAREMIA DETECTION KIT, MODEL JRPD-ASY-0124 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 2007-12-19 under 510(k) number K072547. The device is classified under product code OEH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JBAIDS TULAREMIA DETECTION KIT, MODEL JRPD-ASY-0124?

JBAIDS TULAREMIA DETECTION KIT, MODEL JRPD-ASY-0124 is a medical device that received FDA 510(k) clearance on 2007-12-19. The listed applicant is Idaho Technology, Inc.. The 510(k) number is K072547.

When did JBAIDS TULAREMIA DETECTION KIT, MODEL JRPD-ASY-0124 receive FDA 510(k) clearance?

JBAIDS TULAREMIA DETECTION KIT, MODEL JRPD-ASY-0124 received FDA 510(k) clearance on 2007-12-19, under 510(k) number K072547.

Who is the listed applicant for JBAIDS TULAREMIA DETECTION KIT, MODEL JRPD-ASY-0124?

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 TULAREMIA DETECTION KIT, MODEL JRPD-ASY-0124?

The FDA product code for JBAIDS TULAREMIA DETECTION KIT, MODEL JRPD-ASY-0124 is OEH.

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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 PANELK103207JBAIDS Q FEVER DETECTION KITK110764FILMARRAY RP PANELK103175FILMARRAY RESPIRATORY PANEL (RP)K072631JBAIDS PLAQUE DETECTION KIT, MODEL JRPD-ASY-0123K071188MODIFICATION TO JBAIDS ANTHRAX DETECTION SYSTEM

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Related Devices (Code: OEH)

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.

K131936JBAIDS TULAREMIA DETECTION KITBiofire Diagnostics, 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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