STERRAD BI TEST PACK— 510(k) K921909
Substantially EquivalentJohnson & Johnson Medical, Inc.
FDA 510(k) clearance K921909 for STERRAD BI TEST PACK, Substantially Equivalent on 1993-10-01. Applicant: Johnson & Johnson Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Johnson & Johnson Medical, Inc.
- Product code
- Code FRC
- Device class
- Class 2
- Regulation
- 21 CFR 880.2800
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Arlington, TX, US
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