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FDA 510(k)

7 TRICYCLIC ANTIDE PRESSANTS

K-Number: K802245 · 1980-10-10

ApplicantTechnicon Instruments Corp.
Decision Date1980-10-10
Product CodeLFI
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

7 TRICYCLIC ANTIDE PRESSANTS is the device name listed in this FDA 510(k) record. The listed applicant is Technicon Instruments Corp.. It received FDA 510(k) clearance on 1980-10-10 under 510(k) number K802245. The device is classified under product code LFI. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 7 TRICYCLIC ANTIDE PRESSANTS?

7 TRICYCLIC ANTIDE PRESSANTS is a medical device that received FDA 510(k) clearance on 1980-10-10. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K802245.

When did 7 TRICYCLIC ANTIDE PRESSANTS receive FDA 510(k) clearance?

7 TRICYCLIC ANTIDE PRESSANTS received FDA 510(k) clearance on 1980-10-10, under 510(k) number K802245.

Who is the listed applicant for 7 TRICYCLIC ANTIDE PRESSANTS?

The FDA 510(k) record lists Technicon Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 7 TRICYCLIC ANTIDE PRESSANTS?

The FDA product code for 7 TRICYCLIC ANTIDE PRESSANTS is LFI.

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Related Devices (Code: LFI)

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K941990BENOZODIAZEPINES AND TRICYLIC ANTIDEPRESSANTS BY HPLCBio-RadK941994BENZODIAZEPINES AND TRICYCLIC ANTIDEPRESSANTS BY HPLCBio-RadK934340BIOSITE DIAGNOSTICS - TRIAGE PANEL FOR DRUGS OF ABUSE PLUS TRICYCLIC ANTIDEPRESSANTSBiosite Incorporated

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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