WHIS-RAD TUBSTAND STRUCTURE/MOBILE PATIENT TROLLEY— 510(k) K935649
Substantially EquivalentBennett X-Ray Corp.
FDA 510(k) clearance K935649 for WHIS-RAD TUBSTAND STRUCTURE/MOBILE PATIENT TROLLEY, Substantially Equivalent on 1994-02-09. Applicant: Bennett X-Ray Corp.. Device class: 2.
Clearance details
- Applicant
- Bennett X-Ray Corp.
- Product code
- Code KPR
- Device class
- Class 2
- Regulation
- 21 CFR 892.1680
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Copiague, NY, US
Recent devices under product code KPR
view allMore clearances from Bennett X-Ray Corp.
view all- K964576 — PROFILE MAMMOGRAPHY SYSTEM (M-PRO)
- K952672 — VERTICAL INTEGRATED PERFECT VIEW (VIP) RADIOGRAPHIC SYSTEM
- K944978 — BENNETT X-RAY DIGITAL SPOT IMAGING SYSTEM MODEL M-DSI
- K945962 — BENNETT X-RAY PROFILE POSITIONING PADDLE FOR MAMMOGRAPHY
- K945731 — HFQ HIGH FREQUENCY RADIOGRAPHIC AND FLUROSCOPIC GENERATORS
Adverse events under product code KPR
product code KPR- Other
- 6
- Total
- 6
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.