TRANSPAK (VITREORETINAL INFUSION PAK), MODELS 90000, 90001— 510(k) K000416
Substantially EquivalentRetinalabs.Com
FDA 510(k) clearance K000416 for TRANSPAK (VITREORETINAL INFUSION PAK), MODELS 90000, 90001, Substantially Equivalent on 2000-05-08. Applicant: Retinalabs.Com. Device class: 2.
Clearance details
- Applicant
- Retinalabs.Com
- Product code
- Code MPA
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Atlanta, GA, US
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More clearances from Retinalabs.Com
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- K000457 — VERTEFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 11000 SERIES; PHOTOFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 12000 SERIES
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Data sourced from openFDA. This site is unofficial and independent of the FDA.