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FDA 510(k)

IVSK09 CALIBRATION KIT AN ACCESSORY TO IV7000/7200

K-Number: K890786 · 1989-07-28

ApplicantValleylab, Inc.
Decision Date1989-07-28
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IVSK09 CALIBRATION KIT AN ACCESSORY TO IV7000/7200 is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1989-07-28 under 510(k) number K890786. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IVSK09 CALIBRATION KIT AN ACCESSORY TO IV7000/7200?

IVSK09 CALIBRATION KIT AN ACCESSORY TO IV7000/7200 is a medical device that received FDA 510(k) clearance on 1989-07-28. The listed applicant is Valleylab, Inc.. The 510(k) number is K890786.

When did IVSK09 CALIBRATION KIT AN ACCESSORY TO IV7000/7200 receive FDA 510(k) clearance?

IVSK09 CALIBRATION KIT AN ACCESSORY TO IV7000/7200 received FDA 510(k) clearance on 1989-07-28, under 510(k) number K890786.

Who is the listed applicant for IVSK09 CALIBRATION KIT AN ACCESSORY TO IV7000/7200?

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

What is the FDA product code for IVSK09 CALIBRATION KIT AN ACCESSORY TO IV7000/7200?

The FDA product code for IVSK09 CALIBRATION KIT AN ACCESSORY TO IV7000/7200 is FRN.

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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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