510(k) K771559
K771559 is an FDA 510(k) premarket notification submitted by Miles Laboratories, Inc. for the device "HEMA-TEK II SLIDE STAINER". The FDA issued a decision of Substantially Equivalent on August 25, 1977. The device falls under product code KPA (Slide Stainer, Automated), a Class I device regulated under 21 CFR 864.3800. Miles Laboratories, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 25, 1977
- Date Received
- August 15, 1977
- 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