← Product Code [DAT](/submissions/HE/subpart-h%E2%80%94hematology-kits-and-packages/DAT) · K924892

# FIBRINOSTIKA(R) FGDP MICROELISA SYSTEM (K924892)

_Organon Teknika Corp. · DAT · Apr 21, 1994 · Hematology · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/HE/subpart-h%E2%80%94hematology-kits-and-packages/DAT/K924892

## Device Facts

- **Applicant:** Organon Teknika Corp.
- **Product Code:** [DAT](/submissions/HE/subpart-h%E2%80%94hematology-kits-and-packages/DAT.md)
- **Decision Date:** Apr 21, 1994
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 864.7340
- **Device Class:** Class 2
- **Review Panel:** Hematology

## Regulatory Identification

A fibrinogen determination system is a device that consists of the instruments, reagents, standards, and controls used to determine the fibrinogen levels in disseminated intravascular coagulation (nonlocalized clotting within the blood vessels) and primary fibrinolysis (the dissolution of fibrin in a blood clot).

## Special Controls

*Classification.* Class II (special controls). A control or fibrinogen standard intended for use with a fibrinogen determination system is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 864.9.

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**Source:** [https://fda.innolitics.com/submissions/HE/subpart-h%E2%80%94hematology-kits-and-packages/DAT/K924892](https://fda.innolitics.com/submissions/HE/subpart-h%E2%80%94hematology-kits-and-packages/DAT/K924892)

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