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FDA 510(k)

EMIT(R) II CALIBRATOR A LEVEL 1 & LEVEL 2

K-Number: K902578 · 1990-07-10

ApplicantSyva Co.
Decision Date1990-07-10
Product CodeDKB
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

EMIT(R) II CALIBRATOR A LEVEL 1 & LEVEL 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 1990-07-10 under 510(k) number K902578. The device is classified under product code DKB. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMIT(R) II CALIBRATOR A LEVEL 1 & LEVEL 2?

EMIT(R) II CALIBRATOR A LEVEL 1 & LEVEL 2 is a medical device that received FDA 510(k) clearance on 1990-07-10. The listed applicant is Syva Co.. The 510(k) number is K902578.

When did EMIT(R) II CALIBRATOR A LEVEL 1 & LEVEL 2 receive FDA 510(k) clearance?

EMIT(R) II CALIBRATOR A LEVEL 1 & LEVEL 2 received FDA 510(k) clearance on 1990-07-10, under 510(k) number K902578.

Who is the listed applicant for EMIT(R) II CALIBRATOR A LEVEL 1 & LEVEL 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 EMIT(R) II CALIBRATOR A LEVEL 1 & LEVEL 2?

The FDA product code for EMIT(R) II CALIBRATOR A LEVEL 1 & LEVEL 2 is DKB.

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.

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Related Devices (Code: DKB)

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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