MODEL UST-SSD 880L1-5 TRANESOPHAGEAL PHASED ARRAY— 510(k) K861710
Substantially EquivalentJohnson & Johnson Professionals, Inc.
FDA 510(k) clearance K861710 for MODEL UST-SSD 880L1-5 TRANESOPHAGEAL PHASED ARRAY, Substantially Equivalent on 1986-07-09. Applicant: Johnson & Johnson Professionals, Inc.. Device class: 2.
Clearance details
- Applicant
- Johnson & Johnson Professionals, Inc.
- Product code
- Code DXK
- Device class
- Class 2
- Regulation
- 21 CFR 870.2330
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Ramsey, NJ, US
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