Ats Gram Stain Control Slide
FDA 510(k) K823704 · Alpha-Tec Systems, Inc.
510(k) numberK823704
Submission
- Device name
- Ats Gram Stain Control Slide
- Applicant
- Alpha-Tec Systems, Inc.
Mchenry, IL, US - Received
- December 9, 1982
- Decision date
- January 7, 1983
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- LJG – Quality Control Slides
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 866.2660
- Specialty
- Microbiology
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|---|---|---|---|
| K943228 | Microsporidium Control SetLJG · Traditional | Meridian Diagnostics, Inc. | 10/27/1994SE |
| K924893 | Microsporidium Control SlideLJG · Traditional | Scientific Device Laboratory, Inc. | 01/15/1993SE |
| K890718 | Gram Stain Control SlideLJG · Traditional | Scientific Device Laboratory, Inc. | 03/16/1989SE |
| K890670 | Cryptosporidium Control SlideLJG · Traditional | Scientific Device Laboratory, Inc. | 03/16/1989SE |
| K890616 | Bion Direct Identification Control SlideLJG · Traditional | Bion Ent., Ltd. | 02/17/1989SE |
| K883571 | Histo-Check Parasitic Control SlidesLJG · Traditional | Val Tech Diagnostics, Inc. | 10/06/1988SE |
| K883570 | Histo-Check Fungal Control SlidesLJG · Traditional | Val Tech Diagnostics, Inc. | 10/06/1988SE |
| K883569 | Histo-Check Gram Negative SlidesLJG · Traditional | Val Tech Diagnostics, Inc. | 10/06/1988SE |
| K883568 | Histo-Check Acid Fast SlidesLJG · Traditional | Val Tech Diagnostics, Inc. | 10/06/1988SE |
| K883567 | Histo-Check Legionella Control SlidesLJG · Traditional | Val Tech Diagnostics, Inc. | 10/06/1988SE |
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| K883049 | Ats Para-Set Iodine Alcohol SolutionJTS · Traditional | 08/17/1988SE |
| K883048 | Ats Para-Set Modified Pva Fixative SolutionLDZ · Traditional | 08/17/1988SE |
| K883062 | Ats Schaudinn's Fixative W/Acetic AcidLDW · Traditional | 08/04/1988SE |
| K881949 | Ats Nac-Pac SetJSK · Traditional | 05/25/1988SE |
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Questions and answers
When was Ats Gram Stain Control Slide cleared by the FDA?
Ats Gram Stain Control Slide (K823704) received a 510(k) decision of Substantially Equivalent on January 7, 1983, 29 days after the submission was received.
What is the product code of K823704?
The FDA product code is LJG – Quality Control Slides, a Class I (low risk) device regulated under 21 CFR 866.2660.