Ace Hdl-C Reagent

FDA 510(k) K971526 · Schiapparelli Biosystems, Inc.

Substantially Equivalent

510(k) numberK971526

Submission

Device name
Ace Hdl-C Reagent
Applicant
Schiapparelli Biosystems, Inc.
Fairfield, NJ, US
Received
April 28, 1997
Decision date
May 21, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
LBS – Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl
Device class
Class I (low risk)
Regulation
21 CFR 862.1475
Specialty
Clinical Chemistry

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K973536Ace Phenobarbital Reagent/Aed CalibratorsDLJ · Traditional 11/06/1997SE
K973414Ace Phenytoin Reagent, AED CalibratorsDIP · Traditional 11/04/1997SE
K973535Ace Carbamazepine Reagent/Aed CalibratorsKLT · Traditional 10/20/1997SE
K954179HDL Precipitating ReagentLBR · Traditional 12/11/1995SE

Questions and answers

When was Ace Hdl-C Reagent cleared by the FDA?

Ace Hdl-C Reagent (K971526) received a 510(k) decision of Substantially Equivalent on May 21, 1997, 23 days after the submission was received.

What is the product code of K971526?

The FDA product code is LBS – Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl, a Class I (low risk) device regulated under 21 CFR 862.1475.