GAUZE SPONGE— 510(k) K953812
Substantially EquivalentRemington Medical, Inc.
FDA 510(k) clearance K953812 for GAUZE SPONGE, Substantially Equivalent on 1995-10-02. Applicant: Remington Medical, Inc.. Device class: 1.
Clearance details
- Applicant
- Remington Medical, Inc.
- Product code
- Code KHR
- Device class
- Class 1
- Regulation
- 21 CFR 872.6050
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Atlanta, GA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.