510(k) K832055
K832055 is an FDA 510(k) premarket notification submitted by Syva Co. for the device "EMIT ASSAY AND TOBRAMYCIN". The FDA issued a decision of Substantially Equivalent on August 8, 1983. The device falls under product code LDO (Enzymatic Radiochemical Assay, Tobramycin), a Class II device regulated under 21 CFR 862.3900. Syva Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 8, 1983
- Date Received
- June 27, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Enzymatic Radiochemical Assay, Tobramycin
- Device Class
- Class II
- Regulation Number
- 862.3900
- Review Panel
- TX
- Submission Type