ULTRA-CORE BIOPSY NEEDLES— 510(k) K921418
Substantially EquivalentMedical Device Technologies, Inc.
FDA 510(k) clearance K921418 for ULTRA-CORE BIOPSY NEEDLES, Substantially Equivalent on 1992-06-19. Applicant: Medical Device Technologies, Inc.. Device class: 1.
Clearance details
- Applicant
- Medical Device Technologies, Inc.
- Product code
- Code DWO
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Gainsville, FL, US
Recent devices under product code DWO
view allMore clearances from Medical Device Technologies, Inc.
view all- K101832 — BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENT
- K053518 — INTERV BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR
- K051421 — INTER V BRAND V-MARK BREAST BIOPSY SITE MARKER WITH TITANIUM ANCHOR
- K050873 — CANALIZER HYDROPHILIC GUIDE WIRE
- K043523 — INTERV BRAND SNARELOK BONE MARROW BIOPSY NEEDLE
Data sourced from openFDA. This site is unofficial and independent of the FDA.