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FDA 510(k)

TECHNICON FAST-LC SYS. FOR THEOPHYLLINE

K-Number: K791431 · 1979-10-11

ApplicantTechnicon Instruments Corp.
Decision Date1979-10-11
Product CodeDPA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TECHNICON FAST-LC SYS. FOR THEOPHYLLINE 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 1979-10-11 under 510(k) number K791431. The device is classified under product code DPA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNICON FAST-LC SYS. FOR THEOPHYLLINE?

TECHNICON FAST-LC SYS. FOR THEOPHYLLINE is a medical device that received FDA 510(k) clearance on 1979-10-11. The listed applicant is Technicon Instruments Corp.. The 510(k) number is K791431.

When did TECHNICON FAST-LC SYS. FOR THEOPHYLLINE receive FDA 510(k) clearance?

TECHNICON FAST-LC SYS. FOR THEOPHYLLINE received FDA 510(k) clearance on 1979-10-11, under 510(k) number K791431.

Who is the listed applicant for TECHNICON FAST-LC SYS. FOR THEOPHYLLINE?

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 TECHNICON FAST-LC SYS. FOR THEOPHYLLINE?

The FDA product code for TECHNICON FAST-LC SYS. FOR THEOPHYLLINE is DPA.

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Other records listing Technicon Instruments Corp. as applicant

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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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