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FDA 510(k)

ATOMSPEC GF BLOOD LEAD WORKSTATION

K-Number: K936060 · 1994-09-06

ApplicantThermo Jarrell Ash Corp.Div.Thermo Inst.
Decision Date1994-09-06
Product CodeDOF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

ATOMSPEC GF BLOOD LEAD WORKSTATION is the device name listed in this FDA 510(k) record. The listed applicant is Thermo Jarrell Ash Corp.Div.Thermo Inst.. It received FDA 510(k) clearance on 1994-09-06 under 510(k) number K936060. The device is classified under product code DOF. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATOMSPEC GF BLOOD LEAD WORKSTATION?

ATOMSPEC GF BLOOD LEAD WORKSTATION is a medical device that received FDA 510(k) clearance on 1994-09-06. The listed applicant is Thermo Jarrell Ash Corp.Div.Thermo Inst.. The 510(k) number is K936060.

When did ATOMSPEC GF BLOOD LEAD WORKSTATION receive FDA 510(k) clearance?

ATOMSPEC GF BLOOD LEAD WORKSTATION received FDA 510(k) clearance on 1994-09-06, under 510(k) number K936060.

Who is the listed applicant for ATOMSPEC GF BLOOD LEAD WORKSTATION?

The FDA 510(k) record lists Thermo Jarrell Ash Corp.Div.Thermo Inst. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ATOMSPEC GF BLOOD LEAD WORKSTATION?

The FDA product code for ATOMSPEC GF BLOOD LEAD WORKSTATION is DOF.

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Related Devices (Code: DOF)

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.

K123563LEADCARE (R) ULTRA (TM) BLOOD LEAD TESTING SYSTEMMagellan DiagnosticsK052549LEADCARE II BLOOD LEAD TESTING SYSTEMEsa Biosciences, Inc.K971640LEADCARE BLOOD LEAD TESTING SYSTEMEsa, Inc.K843839STAT/PB REAGENTTri-Tech, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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