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FDA 510(k)

EMIT AND NETILMICIN CONTROL

K-Number: K820323 · 1982-02-23

ApplicantSyva Co.
Decision Date1982-02-23
Product CodeLAS
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

EMIT AND NETILMICIN 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 1982-02-23 under 510(k) number K820323. The device is classified under product code LAS. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMIT AND NETILMICIN CONTROL?

EMIT AND NETILMICIN CONTROL is a medical device that received FDA 510(k) clearance on 1982-02-23. The listed applicant is Syva Co.. The 510(k) number is K820323.

When did EMIT AND NETILMICIN CONTROL receive FDA 510(k) clearance?

EMIT AND NETILMICIN CONTROL received FDA 510(k) clearance on 1982-02-23, under 510(k) number K820323.

Who is the listed applicant for EMIT AND NETILMICIN 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 AND NETILMICIN CONTROL?

The FDA product code for EMIT AND NETILMICIN CONTROL is LAS.

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: LAS)

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

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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