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FDA 510(k)

EMIT-CAD PROCAINAMIDE/N-ACETYL. CONTROL

K-Number: K811618 · 1981-06-25

ApplicantSyva Co.
Decision Date1981-06-25
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

EMIT-CAD PROCAINAMIDE/N-ACETYL. 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 1981-06-25 under 510(k) number K811618. The device is classified under product code DIF. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMIT-CAD PROCAINAMIDE/N-ACETYL. CONTROL?

EMIT-CAD PROCAINAMIDE/N-ACETYL. CONTROL is a medical device that received FDA 510(k) clearance on 1981-06-25. The listed applicant is Syva Co.. The 510(k) number is K811618.

When did EMIT-CAD PROCAINAMIDE/N-ACETYL. CONTROL receive FDA 510(k) clearance?

EMIT-CAD PROCAINAMIDE/N-ACETYL. CONTROL received FDA 510(k) clearance on 1981-06-25, under 510(k) number K811618.

Who is the listed applicant for EMIT-CAD PROCAINAMIDE/N-ACETYL. 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 EMIT-CAD PROCAINAMIDE/N-ACETYL. CONTROL?

The FDA product code for EMIT-CAD PROCAINAMIDE/N-ACETYL. CONTROL is DIF.

Related Clinical Trials

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.

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.

View all 448 devices →

Related Devices (Code: DIF)

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.

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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