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FDA 510(k)

SYVA ADVANCE STANDARDIZATION KIT #2

K-Number: K821937 · 1982-07-16

ApplicantSyva Co.
Decision Date1982-07-16
Product CodeJIS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SYVA ADVANCE STANDARDIZATION KIT #2 is the device name listed in this FDA 510(k) record. The listed applicant is Syva Co.. It received FDA 510(k) clearance on 1982-07-16 under 510(k) number K821937. The device is classified under product code JIS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYVA ADVANCE STANDARDIZATION KIT #2?

SYVA ADVANCE STANDARDIZATION KIT #2 is a medical device that received FDA 510(k) clearance on 1982-07-16. The listed applicant is Syva Co.. The 510(k) number is K821937.

When did SYVA ADVANCE STANDARDIZATION KIT #2 receive FDA 510(k) clearance?

SYVA ADVANCE STANDARDIZATION KIT #2 received FDA 510(k) clearance on 1982-07-16, under 510(k) number K821937.

Who is the listed applicant for SYVA ADVANCE STANDARDIZATION KIT #2?

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 SYVA ADVANCE STANDARDIZATION KIT #2?

The FDA product code for SYVA ADVANCE STANDARDIZATION KIT #2 is JIS.

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Other records listing Syva Co. as applicant

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Related Devices (Code: JIS)

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.

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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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