INTERSPEC APOGEE, MODIFICATION— 510(k) K910049
Substantially EquivalentInterspec, Inc.
FDA 510(k) clearance K910049 for INTERSPEC APOGEE, MODIFICATION, Substantially Equivalent on 1991-04-29. Applicant: Interspec, Inc.. Device class: 2.
Clearance details
- Applicant
- Interspec, Inc.
- Product code
- Code DPW
- Device class
- Class 2
- Regulation
- 21 CFR 870.2100
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Ambler, PA, US
Recent devices under product code DPW
view allMore clearances from Interspec, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.