MODIFIED LABELING TO THE SPAND-GEL GRANULATED GEL— 510(k) K895819
Substantially Equivalent for Some IndicationsMedi-Tech, Inc.
FDA 510(k) clearance K895819 for MODIFIED LABELING TO THE SPAND-GEL GRANULATED GEL, Substantially Equivalent for Some Indications on 1989-11-02. Applicant: Medi-Tech, Inc.. Device class: 1.
Clearance details
- Applicant
- Medi-Tech, Inc.
- Product code
- Code KMF
- Device class
- Class 1
- Regulation
- 21 CFR 880.5090
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent for Some Indications
- Clearance type
- Traditional
- Location
- Brooklyn, NY, US
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