← Product Code [GJT](/submissions/HE/subpart-h%E2%80%94hematology-kits-and-packages/GJT) · K962671

# STA-VWF CALIBRATOR KIT (K962671)

_American Bioproducts Co. · GJT · Sep 13, 1996 · Hematology · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/HE/subpart-h%E2%80%94hematology-kits-and-packages/GJT/K962671

## Device Facts

- **Applicant:** American Bioproducts Co.
- **Product Code:** [GJT](/submissions/HE/subpart-h%E2%80%94hematology-kits-and-packages/GJT.md)
- **Decision Date:** Sep 13, 1996
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 864.7290
- **Device Class:** Class 2
- **Review Panel:** Hematology

## Indications for Use

The STA®-vWF Calibrator is a citrated human plasma containing von Willebrand Factor (vWF) at the normal level, intended for use as a calibration plasma for the assay of vWF antigen by the immuno-turbidimetric method performed on the STA® analyzer (Diagnostica Stago, France; K942117).

## Device Story

STA®-vWF Calibrator consists of freeze-dried citrated human plasma containing normal levels of von Willebrand Factor (vWF). Used in clinical laboratory settings by trained technicians to calibrate immuno-turbidimetric vWF antigen assays on the STA® analyzer. Each lot is assigned a vWF value via internal reference calibrated against the 3rd International Standard 91/666. Provided in 6 x 1-ml vials; requires reconstitution. Stability: 24 months at 2-8°C; 4 hours on-board analyzer. Output is a reference value used to establish calibration curves for patient sample testing, ensuring accurate quantification of vWF antigen levels.

## Clinical Evidence

Bench testing only; calibration values established via traceability to the 3rd International Standard 91/666.

## Technological Characteristics

Citrated human plasma; freeze-dried form; immuno-turbidimetric assay calibration; stored 2-8°C; 4-hour on-board stability.

## Reference Devices

- STA® analyzer ([K942117](/device/K942117.md))
- 3rd International Standard 91/666 for Factor VIII and von Willebrand Factor

## Submission Summary (Full Text)

> This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com.
>
> Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/).

{0}

SEP 13 1996
K962671
Page 16 of 16

AMERICAN BIOPRODUCTS COMPANY
Premarket 510(k) Notification
STA®-vWF Calibrator Kit

## VII. SAFETY AND EFFECTIVENESS SUMMARY

The STA®-vWF Calibrator is a citrated human plasma containing von Willebrand Factor (vWF) at the normal level, intended for use as a calibration plasma for the assay of vWF antigen by the immuno-turbidimetric method performed on the STA® analyzer (Diagnostica Stago, France; K942117).

Each manufactured lot of STA®-vWF Calibrator is assigned a vWF value which is determined with an internal vWF reference that has been assayed against the third International Standard 91/666 for Factor VIII and von Willebrand Factor established in 1992.

Each STA®-vWF Calibrator kit provides 6 x 1-ml vials of citrated human plasma in freeze-dried form. The vWF value of each lot is provided in the Assay Value insert supplied with each kit. The freeze-dried reagent in intact vials is stable for 24 months after the date of manufacture, when stored at 2°-8°C; the reconstituted plasma remains stable for 4 hours on board the STA® analyzer.

---

**Source:** [https://fda.innolitics.com/submissions/HE/subpart-h%E2%80%94hematology-kits-and-packages/GJT/K962671](https://fda.innolitics.com/submissions/HE/subpart-h%E2%80%94hematology-kits-and-packages/GJT/K962671)

**Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact).

**Cite:** Innolitics at https://innolitics.com
