Multi-Probe Head Plus
FDA 510(k) K892369 · Hamilton Co.
510(k) numberK892369
Submission
- Device name
- Multi-Probe Head Plus
- Applicant
- Hamilton Co.
Reno, NV, US - Received
- April 6, 1989
- Decision date
- June 2, 1989
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- JTC – Device, Microtiter Diluting/Dispensing
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 866.2500
- Specialty
- Microbiology
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Questions and answers
When was Multi-Probe Head Plus cleared by the FDA?
Multi-Probe Head Plus (K892369) received a 510(k) decision of Substantially Equivalent on June 2, 1989, 57 days after the submission was received.
What is the product code of K892369?
The FDA product code is JTC – Device, Microtiter Diluting/Dispensing, a Class I (low risk) device regulated under 21 CFR 866.2500.