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FDA 510(k)

(SPAG) MODEL SPAG-2 6000 SERIES

K-Number: K871427 · 1987-10-06

ApplicantViratek, Inc.
Decision Date1987-10-06
Product CodeCAF
Advisory CommitteeAN
DecisionUnknown

Device Summary

(SPAG) MODEL SPAG-2 6000 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Viratek, Inc.. It received FDA 510(k) clearance on 1987-10-06 under 510(k) number K871427. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the (SPAG) MODEL SPAG-2 6000 SERIES?

(SPAG) MODEL SPAG-2 6000 SERIES is a medical device that received FDA 510(k) clearance on 1987-10-06. The listed applicant is Viratek, Inc.. The 510(k) number is K871427.

When did (SPAG) MODEL SPAG-2 6000 SERIES receive FDA 510(k) clearance?

(SPAG) MODEL SPAG-2 6000 SERIES received FDA 510(k) clearance on 1987-10-06, under 510(k) number K871427.

Who is the listed applicant for (SPAG) MODEL SPAG-2 6000 SERIES?

The FDA 510(k) record lists Viratek, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for (SPAG) MODEL SPAG-2 6000 SERIES?

The FDA product code for (SPAG) MODEL SPAG-2 6000 SERIES is CAF.

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Other records listing Viratek, Inc. as applicant

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Related Devices (Code: CAF)

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Official Source

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