DU PONT STERICELL CELL CULTURE SYSTEM— 510(k) K871324
Substantially EquivalentE.I. Dupont DE Nemours & Co., Inc.
FDA 510(k) clearance K871324 for DU PONT STERICELL CELL CULTURE SYSTEM, Substantially Equivalent on 1987-04-14. Applicant: E.I. Dupont DE Nemours & Co., Inc.. Device class: 1.
Clearance details
- Applicant
- E.I. Dupont DE Nemours & Co., Inc.
- Product code
- Code KJA
- Device class
- Class 1
- Regulation
- 21 CFR 864.2240
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wilmington, DE, US
Recent devices under product code KJA
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