SPOROX— 510(k) K970230
Substantially EquivalentReckitt Benckiser, Inc.
FDA 510(k) clearance K970230 for SPOROX, Substantially Equivalent on 1997-10-29. Applicant: Reckitt Benckiser, Inc.. Device class: 2.
Clearance details
- Applicant
- Reckitt Benckiser, Inc.
- Product code
- Code MED
- Device class
- Class 2
- Regulation
- 21 CFR 880.6885
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Montvale, NJ, US
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