DU PONT DIMENSION PSEUDOCHOLINESTERASE METHOD— 510(k) K883890
Substantially EquivalentE.I. Dupont DE Nemours & Co., Inc.
FDA 510(k) clearance K883890 for DU PONT DIMENSION PSEUDOCHOLINESTERASE METHOD, Substantially Equivalent on 1988-11-29. Applicant: E.I. Dupont DE Nemours & Co., Inc.. Device class: 1.
Clearance details
- Applicant
- E.I. Dupont DE Nemours & Co., Inc.
- Product code
- Code DIH
- Device class
- Class 1
- Regulation
- 21 CFR 862.3240
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wilmington, DE, US
Recent devices under product code DIH
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