MAX-I-PROBE PERIDONTAL/ENDODONTIC PROBE(TM) (MODI)— 510(k) K864307
Substantially EquivalentSmith & Nephew, Inc.
FDA 510(k) clearance K864307 for MAX-I-PROBE PERIDONTAL/ENDODONTIC PROBE(TM) (MODI), Substantially Equivalent on 1986-11-18. Applicant: Smith & Nephew, Inc.. Device class: 1.
Clearance details
- Applicant
- Smith & Nephew, Inc.
- Product code
- Code EIC
- Device class
- Class 1
- Regulation
- 21 CFR 872.4565
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Chicago, IL, US
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