THE ORIGINAL PULSE-PAK— 510(k) K892639
Substantially EquivalentJones Sales Co.
FDA 510(k) clearance K892639 for THE ORIGINAL PULSE-PAK, Substantially Equivalent on 1989-10-05. Applicant: Jones Sales Co.. Device class: 2.
Clearance details
- Applicant
- Jones Sales Co.
- Product code
- Code NFB
- Device class
- Class 2
- Regulation
- 21 CFR 868.5905
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Canal Winchester, OH, US
Recent devices under product code NFB
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