510(k) K832994
K832994 is an FDA 510(k) premarket notification submitted by Innovative Medical Systems, Inc. for the device "MIDAS 6000 AUTOMATIC STAINER". The FDA issued a decision of Substantially Equivalent on September 29, 1983. The device falls under product code KPA (Slide Stainer, Automated), a Class I device regulated under 21 CFR 864.3800. Innovative Medical Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 29, 1983
- Date Received
- September 2, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Slide Stainer, Automated
- Device Class
- Class I
- Regulation Number
- 864.3800
- Review Panel
- PA
- Submission Type