510(k) K952501
K952501 is an FDA 510(k) premarket notification submitted by Chimera Research & Chemical, Inc. for the device "TOX PERFECT B TUBES AND REAGENTS". The FDA issued a decision of Substantially Equivalent on August 24, 1995. The device falls under product code DPM (Columns, Liquid Chromatography), a Class I device regulated under 21 CFR 862.2260. Chimera Research & Chemical, Inc. has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 24, 1995
- Date Received
- May 30, 1995
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Columns, Liquid Chromatography
- Device Class
- Class I
- Regulation Number
- 862.2260
- Review Panel
- TX
- Submission Type