510(k) K930166
K930166 is an FDA 510(k) premarket notification submitted by Em Diagnostic Systems, Inc. for the device "IRON TEST #'S 42376/93,42324/R1A,42324/R1B,42324/R". The FDA issued a decision of Substantially Equivalent on April 21, 1993. The device falls under product code JIY (Photometric Method, Iron (Non-Heme)), a Class I device regulated under 21 CFR 862.1410. Em Diagnostic Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 21, 1993
- Date Received
- January 13, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Photometric Method, Iron (Non-Heme)
- Device Class
- Class I
- Regulation Number
- 862.1410
- Review Panel
- CH
- Submission Type