510(k) K770353
K770353 is an FDA 510(k) premarket notification submitted by Inhal-O-Tech Medical Plastic for the device "DISPOSABLE TEMPERATURE PROBE". The FDA issued a decision of Substantially Equivalent on March 16, 1977. The device falls under product code KPD (Strip, Temperature, Forehead, Liquid Crystal), a Class II device regulated under 21 CFR 880.2200. Inhal-O-Tech Medical Plastic has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 16, 1977
- Date Received
- February 22, 1977
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Strip, Temperature, Forehead, Liquid Crystal
- Device Class
- Class II
- Regulation Number
- 880.2200
- Review Panel
- HO
- Submission Type