510(k) K872330
K872330 is an FDA 510(k) premarket notification submitted by Em Diagnostic Systems, Inc. for the device "EMDS SALICYLATE (SAL) TESTPACKS, ITEM NO. 67694/95". The FDA issued a decision of Substantially Equivalent on July 9, 1987. The device falls under product code DKJ (Colorimetry, Salicylate), a Class II device regulated under 21 CFR 862.3830. Em Diagnostic Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 9, 1987
- Date Received
- June 17, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Colorimetry, Salicylate
- Device Class
- Class II
- Regulation Number
- 862.3830
- Review Panel
- TX
- Submission Type