← Product Code [JTR](/submissions/MI/subpart-c%E2%80%94microbiology-devices/JTR) · K821660

# BIO-CHECK GRAM STAIN CONTROL (K821660)

_American Scientific Products · JTR · Jun 25, 1982 · Microbiology · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/MI/subpart-c%E2%80%94microbiology-devices/JTR/K821660

## Device Facts

- **Applicant:** American Scientific Products
- **Product Code:** [JTR](/submissions/MI/subpart-c%E2%80%94microbiology-devices/JTR.md)
- **Decision Date:** Jun 25, 1982
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 866.2480
- **Device Class:** Class 1
- **Review Panel:** Microbiology

## Regulatory Identification

A quality control kit for culture media is a device that consists of paper discs (or other suitable materials), each impregnated with a specified, freeze-dried, viable microorganism, intended for medical purposes to determine if a given culture medium is able to support the growth of that microorganism. The device aids in the diagnosis of disease caused by pathogenic microorganisms and also provides epidemiological information on these diseases.

---

**Source:** [https://fda.innolitics.com/submissions/MI/subpart-c%E2%80%94microbiology-devices/JTR/K821660](https://fda.innolitics.com/submissions/MI/subpart-c%E2%80%94microbiology-devices/JTR/K821660)

**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
