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FDA 510(k)

ADVANCE SYS. EMIT-CAD LIDOCAINE CONTROL

K-Number: K823865 · 1983-01-14

ApplicantSyva Co.
Decision Date1983-01-14
Product CodeLAX
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

ADVANCE SYS. EMIT-CAD LIDOCAINE CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Syva Co.. It received FDA 510(k) clearance on 1983-01-14 under 510(k) number K823865. The device is classified under product code LAX. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADVANCE SYS. EMIT-CAD LIDOCAINE CONTROL?

ADVANCE SYS. EMIT-CAD LIDOCAINE CONTROL is a medical device that received FDA 510(k) clearance on 1983-01-14. The listed applicant is Syva Co.. The 510(k) number is K823865.

When did ADVANCE SYS. EMIT-CAD LIDOCAINE CONTROL receive FDA 510(k) clearance?

ADVANCE SYS. EMIT-CAD LIDOCAINE CONTROL received FDA 510(k) clearance on 1983-01-14, under 510(k) number K823865.

Who is the listed applicant for ADVANCE SYS. EMIT-CAD LIDOCAINE CONTROL?

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

What is the FDA product code for ADVANCE SYS. EMIT-CAD LIDOCAINE CONTROL?

The FDA product code for ADVANCE SYS. EMIT-CAD LIDOCAINE CONTROL is LAX.

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Other records listing Syva Co. 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.

K011878EMIT (R) TOX SALICYLIC ASSAY, MODEL 7SO19UL, EMIT (R) TOX SALICYLIC ACID CALIBRATORS, MODEL 7S109ULK012257EMIT II PLUS MONOCLONAL AMPHETAMINE/METHAMPHETAMINE ASSAY MODEL OSR9C229K011947EMIT 2000 VALPROIC ACID ASSAY, MODEL OSR4G229ULK011528EMIT 2000 PHENOBARBITAL ASSAY, MODEL OSR4D229K011347EMIT 2000 PHENYTOIN ASSAY, MODEL 0SR4A229K993980SYVA EMIT II PLUS ETHYL ALCOHOL ASSAY, MODELS 9K309UL/9K409UL

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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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