510(k) K760788
K760788 is an FDA 510(k) premarket notification submitted by Corning Medical & Scientific for the device "PH METER-125 (.01 PH)". The FDA issued a decision of Substantially Equivalent on November 16, 1976. The device falls under product code JQY (Ph Meter), a Class I device regulated under 21 CFR 862.2050. Corning Medical & Scientific has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 16, 1976
- Date Received
- September 10, 1976
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Ph Meter
- Device Class
- Class I
- Regulation Number
- 862.2050
- Review Panel
- CH
- Submission Type