Gill's Hematoxylin #3
FDA 510(k) K810760 · Surgipath
510(k) numberK810760
Submission
- Device name
- Gill's Hematoxylin #3
- Applicant
- Surgipath
Mchenry, IL, US - Received
- March 20, 1981
- Decision date
- April 14, 1981
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
More from Surgipath
| 510(k) | Device | Decision |
|---|---|---|
| K820027 | Modified Ea 50HZJ · Traditional | 02/04/1982SE |
| K812940 | 10% Neutral Buffered Formalin ConcentIFP · Traditional | 12/10/1981SE |
| K812087 | Ea 50HZJ · Traditional | 08/13/1981SE |
| K812086 | Ea 65HZJ · Traditional | 08/13/1981SE |
| K811826 | Eosin YHYB · Traditional | 07/10/1981SE |
| K811825 | Orange G-6HZH · Traditional | 07/10/1981SE |
| K810836 | Decalcifier IIKDX · Traditional | 04/23/1981SE |
| K810759 | Gill's Hematoxylin #2HYJ · Traditional | 04/14/1981SE |
| K810758 | Gill's Hematoxylin #1HYJ · Traditional | 04/14/1981SE |
| K810733 | Harris HematoxylinHYK · Traditional | 04/14/1981SE |
Questions and answers
When was Gill's Hematoxylin #3 cleared by the FDA?
Gill's Hematoxylin #3 (K810760) received a 510(k) decision of Substantially Equivalent on April 14, 1981, 25 days after the submission was received.