P.R.G. PERCUTANEOUS REPLACEMENT GASTROSTOMY— 510(k) K900884
UnknownApplied Medical Technologies
FDA 510(k) clearance K900884 for P.R.G. PERCUTANEOUS REPLACEMENT GASTROSTOMY, Unknown on 1990-07-02. Applicant: Applied Medical Technologies. Device class: 2.
Clearance details
- Applicant
- Applied Medical Technologies
- Product code
- Code KGC
- Device class
- Class 2
- Regulation
- 21 CFR 876.5980
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Independence, OH, US
Recent devices under product code KGC
view allMore clearances from Applied Medical Technologies
view all- K971434 — A.M.T. G-TUBE BALLOON REPLACEMENT GASTROSTOMY FEEDING DEVICE
- K972478 — PRE-LOADED REPLACEMENT G-TUBES AND ACCESSORIES
- K973893 — AMT BALLOON STOMA MEASURING DEVICES, AMT BALLOON MEASURING DEVICE, AMT BALLOON MEASURING DEVICE WITH STOP VALVE, AMY BAE
- K971757 — LOW PROFILE FEEDING SET ACCESSORY
- K971758 — CAUTERIZATION SMOKE EVACUATOR
Adverse events under product code KGC
product code KGC- Death
- 7
- Total
- 7
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.