NON-STERILE CLINICAL STYLE PARADERM GLOVE LINER— 510(k) K910890
Substantially EquivalentLovell-Schenck, Inc.
FDA 510(k) clearance K910890 for NON-STERILE CLINICAL STYLE PARADERM GLOVE LINER, Substantially Equivalent on 1991-06-27. Applicant: Lovell-Schenck, Inc.. Device class: 1.
Clearance details
- Applicant
- Lovell-Schenck, Inc.
- Product code
- Code LYU
- Device class
- Class 1
- Regulation
- 21 CFR 878.4040
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Charlotte, NC, US
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