MILLEX, DUALEX (PLUS, ULTRA)— 510(k) K934069
Substantially EquivalentMillipore Corp.
FDA 510(k) clearance K934069 for MILLEX, DUALEX (PLUS, ULTRA), Substantially Equivalent on 1994-04-21. Applicant: Millipore Corp.. Device class: 2.
Clearance details
- Applicant
- Millipore Corp.
- Product code
- Code FIB
- Device class
- Class 2
- Regulation
- 21 CFR 876.5820
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bedford, MA, US
Recent devices under product code FIB
view all- K240164 — NovaLine SP-C35 Transducer Protector (956007)
- K072988 — NIPRO TRANSDUCER PROTECTOR TP-SURE, MODEL TPSURE+1
- K001971 — HEMODIALYSIS TUBING SETS
- K010264 — NIPRO BLOOD TUBING SET FOR HEMODIALYSIS WITH TRANSDUCER PROTECTORS AND PRIMING SET
- K001465 — NIPRO BLOOD TUBING SET FOR HEMODIALYSIS WITH TRANSDUCER PROTECTORS AND PRIMING SET
More clearances from Millipore Corp.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.