SPONGETRAC— 510(k) K964181
Substantially EquivalentSurgitrac Corp.
FDA 510(k) clearance K964181 for SPONGETRAC, Substantially Equivalent on 1997-02-26. Applicant: Surgitrac Corp.. Device class: 1.
Clearance details
- Applicant
- Surgitrac Corp.
- Product code
- Code MRL
- Device class
- Class 1
- Regulation
- 21 CFR 880.2740
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.