CLEM TM— 510(k) K902788
Substantially EquivalentArbo Medical, Inc.
FDA 510(k) clearance K902788 for CLEM TM, Substantially Equivalent on 1990-09-12. Applicant: Arbo Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Arbo Medical, Inc.
- 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
- Ann Arbor, MI, 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 Arbo Medical, Inc.
view all- K940323 — ARBO DIAGNOSTIC ECG PATIENT CABLES & LEADWIRES ARBO SHIELDED MULTI-LEAD CABLE & LEAD SYSTEM
- K935437 — ARBO H85V/H87V/H27V DISPOS MONIT ELECTRODES
- K942905 — DISPOSABLE TEMPERATURE PROBE COVER
- K940302 — ARBO MONITRING SAFETY CABLE & LEAD WIRE SYSTEMS/ARBO UNSHEILDED SAFETY CABLE & LEAD SYSTEM
- K940322 — ARBO VS MONITOR CABLE & LEADWIRE SYSTEM ARBO SHIELDED SAFETY CABLE & LEAD WIRE
Data sourced from openFDA. This site is unofficial and independent of the FDA.