Incstar 25-HYDROXYVITMIN D 1251 Ria

FDA 510(k) K953567 · Incstar Corp.

Substantially Equivalent

510(k) numberK953567

Submission

Device name
Incstar 25-HYDROXYVITMIN D 1251 Ria
Applicant
Incstar Corp.
Stillwater, MN, US
Received
July 31, 1995
Decision date
September 25, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MRG – System, Test, Vitamin D
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1825
Specialty
Clinical Chemistry

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Questions and answers

When was Incstar 25-HYDROXYVITMIN D 1251 Ria cleared by the FDA?

Incstar 25-HYDROXYVITMIN D 1251 Ria (K953567) received a 510(k) decision of Substantially Equivalent on September 25, 1996, 422 days after the submission was received.

What is the product code of K953567?

The FDA product code is MRG – System, Test, Vitamin D, a Class II (moderate risk) device regulated under 21 CFR 862.1825.