510(k) K830405
K830405 is an FDA 510(k) premarket notification submitted by Bionetic Laboratory Products for the device "LBI-100 37DEGREES INCUBATOR". The FDA issued a decision of Substantially Equivalent on March 10, 1983. The device falls under product code JTQ (Bath, Incubators/Water, All), a Class I device regulated under 21 CFR 866.2540. Bionetic Laboratory Products has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 10, 1983
- Date Received
- February 7, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Bath, Incubators/Water, All
- Device Class
- Class I
- Regulation Number
- 866.2540
- Review Panel
- MI
- Submission Type