TECNOL ISLAND WOUND DRESSING— 510(k) K954033
Substantially Equivalent for Some IndicationsTecnol Medical Products, Inc.
FDA 510(k) clearance K954033 for TECNOL ISLAND WOUND DRESSING, Substantially Equivalent for Some Indications on 1995-09-22. Applicant: Tecnol Medical Products, Inc.. Device class: Unclassified.
Clearance details
- Applicant
- Tecnol Medical Products, Inc.
- Product code
- Code MGP
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent for Some Indications
- Clearance type
- Traditional
- Location
- Fort Worth, TX, US
Recent devices under product code MGP
view allMore clearances from Tecnol Medical Products, Inc.
view all- K974068 — PFR95 PARTICULATE FILTER RESPIRATOR AND SURGICAL MASK REGULAR SIZE, PFR95 PARTICULATE FILTER RESPIRATOR AND SURGICAL
- K970448 — PCM 2000; ISOLAIR APR MODEL 2735
- K963552 — QUICK RELEASE LIMB HOLDER (24442,24442-050,24442-350)
- K963559 — WRPAROUND LIMB HOLDER (24446,24446-350,24447-010,24449-010)
- K963564 — PERSONAL LIMB HOLDER (24444-200,300,24444-KIT)
Adverse events under product code MGP
product code MGP- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.