510(k) K935531
K935531 is an FDA 510(k) premarket notification submitted by Puritas Health Care, Inc. for the device "OP-FLEX SUMP SUCTION SET WITH DIFFUSER TIP". The FDA issued a decision of Substantially Equivalent on May 5, 1994. The device falls under product code GBX (Catheter, Irrigation), a Class I device regulated under 21 CFR 878.4200. Puritas Health Care, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 5, 1994
- Date Received
- November 16, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Irrigation
- Device Class
- Class I
- Regulation Number
- 878.4200
- Review Panel
- SU
- Submission Type