ulrich Transfer Set— 510(k) K161723
Substantially EquivalentUlrich GmbH & Co. KG
FDA 510(k) clearance K161723 for ulrich Transfer Set, Substantially Equivalent on 2016-12-21. Applicant: Ulrich GmbH & Co. KG. Device class: 2.
Clearance details
- Applicant
- Ulrich GmbH & Co. KG
- Product code
- Code PQH
- Device class
- Class 2
- Regulation
- 21 CFR 880.5440
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Ulm, DE
Recent devices under product code PQH
view allMore clearances from Ulrich GmbH & Co. KG
view all- K252281 — ulricheasyINJECT Max 2M (XD 10140); ulricheasyINJECT Max 3 (XD 10150); ulricheasyINJECT Max 3 (XD 10180)
- K251295 — ulrichINJECT CT Motion (XD 8000)
- K241850 — ulricheasyINJECT Max 2M (XD 10140); ulricheasyINJECT Max 3 (XD 10150); ulricheasyINJECT Max 3 (XD 10180)
- K233737 — ulricheasyINJECT Max 2M (XD 10140); ulricheasyINJECT Max 3 (XD 10150); ulricheasyINJECT Max 3 (XD 10180)
- K210541 — ulrichINJECT CT motion
Data sourced from openFDA. This site is unofficial and independent of the FDA.