ADULT INCONTINET BRIEF— 510(k) K821397
Substantially EquivalentJohnson & Johnson Professionals, Inc.
FDA 510(k) clearance K821397 for ADULT INCONTINET BRIEF, Substantially Equivalent on 1982-05-24. Applicant: Johnson & Johnson Professionals, Inc.. Device class: 1.
Clearance details
- Applicant
- Johnson & Johnson Professionals, Inc.
- Product code
- Code EYQ
- Device class
- Class 1
- Regulation
- 21 CFR 876.5920
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Raynham, MA, US
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