TUTTNAUER MINI CONTAINER CASSETTE, TUTTNAUER STANDARD CASE CASSETTE— 510(k) K990761
Substantially EquivalentTuttnauer U.S.A Co, Ltd.
FDA 510(k) clearance K990761 for TUTTNAUER MINI CONTAINER CASSETTE, TUTTNAUER STANDARD CASE CASSETTE, Substantially Equivalent on 1999-07-09. Applicant: Tuttnauer U.S.A Co, Ltd.. Device class: 2.
Clearance details
- Applicant
- Tuttnauer U.S.A Co, Ltd.
- Product code
- Code FRG
- Device class
- Class 2
- Regulation
- 21 CFR 880.6850
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington D.C., DC, US
Recent devices under product code FRG
view allMore clearances from Tuttnauer U.S.A Co, Ltd.
view all- K232658 — T-Top 10 & T-Top T-Top 11
- K143311 — Pre-vacuum Tabletop Autoclave
- K090783 — TUTTNAUER ELARA-11 PRE-VACUUM TABLETOP AUTOCLAVE
- K032192 — PRE-VACUUM AUTOCLAVE WITH STEAM GENERATOR AND VERTICAL SLIDING DOOR, MODELS 4472 EP-1V AND 5596 EP-1V
- K021504 — TUTTNAUER EHS SERIES TABLE-TOP AUTOCLAVE, MODEL 2540
Adverse events under product code FRG
product code FRG- Other
- 3
- Total
- 3
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.