Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

EMIT-ST SERUM CONTROLS

K-Number: K810468 · 1981-03-06

ApplicantSyva Co.
Decision Date1981-03-06
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

EMIT-ST SERUM CONTROLS is the device name listed in this FDA 510(k) record. The listed applicant is Syva Co.. It received FDA 510(k) clearance on 1981-03-06 under 510(k) number K810468. 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-ST SERUM CONTROLS?

EMIT-ST SERUM CONTROLS is a medical device that received FDA 510(k) clearance on 1981-03-06. The listed applicant is Syva Co.. The 510(k) number is K810468.

When did EMIT-ST SERUM CONTROLS receive FDA 510(k) clearance?

EMIT-ST SERUM CONTROLS received FDA 510(k) clearance on 1981-03-06, under 510(k) number K810468.

Who is the listed applicant for EMIT-ST SERUM CONTROLS?

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-ST SERUM CONTROLS?

The FDA product code for EMIT-ST SERUM CONTROLS 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑