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FDA 510(k)

SYVA MYCOTRANS MYCOPLASMA TRANSPORT SYSTEM

K-Number: K854061 · 1985-10-23

ApplicantSyva Co.
Decision Date1985-10-23
Product CodeJSM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SYVA MYCOTRANS MYCOPLASMA TRANSPORT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Syva Co.. It received FDA 510(k) clearance on 1985-10-23 under 510(k) number K854061. The device is classified under product code JSM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYVA MYCOTRANS MYCOPLASMA TRANSPORT SYSTEM?

SYVA MYCOTRANS MYCOPLASMA TRANSPORT SYSTEM is a medical device that received FDA 510(k) clearance on 1985-10-23. The listed applicant is Syva Co.. The 510(k) number is K854061.

When did SYVA MYCOTRANS MYCOPLASMA TRANSPORT SYSTEM receive FDA 510(k) clearance?

SYVA MYCOTRANS MYCOPLASMA TRANSPORT SYSTEM received FDA 510(k) clearance on 1985-10-23, under 510(k) number K854061.

Who is the listed applicant for SYVA MYCOTRANS MYCOPLASMA TRANSPORT SYSTEM?

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 MYCOTRANS MYCOPLASMA TRANSPORT SYSTEM?

The FDA product code for SYVA MYCOTRANS MYCOPLASMA TRANSPORT SYSTEM is JSM.

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: JSM)

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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