BARD INTRA-ABDOMINAL PRESSURE MONITORING DEVICE, MODEL IAP-001— 510(k) K070201
Substantially EquivalentC.R. Bard, Inc.
FDA 510(k) clearance K070201 for BARD INTRA-ABDOMINAL PRESSURE MONITORING DEVICE, MODEL IAP-001, Substantially Equivalent on 2007-08-01. Applicant: C.R. Bard, Inc.. Device class: Unclassified.
Clearance details
- Applicant
- C.R. Bard, Inc.
- Product code
- Code PHU
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Covington, GA, US
Recent devices under product code PHU
view allMore clearances from C.R. Bard, Inc.
view all- K253514 — Minnesota Four-Lumen Esophagogastric Tamponade Tube - 18 French (0092220) +2 more
- K254076 — BD Touchless Plus Unisex Pre-Lubricated Urethral Catheter Kit
- K252971 — Elyra Thulium Fiber Laser System and Elyra Plus Thulium Fiber Laser System (Laser, Fibers, and Accessories)
- K251864 — Rubber Utility Catheter
- K251186 — Bard® Temporary Pacing Electrode Catheter Needle / Cannula (Introducer)
Recalls naming K070201
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K070201.
Data sourced from openFDA. This site is unofficial and independent of the FDA.