LACERATION REPAIR TRAY— 510(k) K921988
UnknownCypress Medical Products, Ltd.
FDA 510(k) clearance K921988 for LACERATION REPAIR TRAY, Unknown on 1992-11-19. Applicant: Cypress Medical Products, Ltd.. Device class: 1.
Clearance details
- Applicant
- Cypress Medical Products, Ltd.
- Product code
- Code MDM
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Mc Henry, IL, US
Recent devices under product code MDM
view allMore clearances from Cypress Medical Products, Ltd.
view all- K021676 — CYPRESS MEDICAL PRODUCTS, LP DISPOSABLE VAGINAL SPECULUM, NON-METAL
- K012282 — STERILE POWDER FREE SYNTHETIC VINYL PATIENT EXAM GLOVE
- K972899 — CYPRESS MEDICAL PRODUCTS ANEROID SPHYGMOMANOMETER
- K972849 — ISOSAFE EARLOOP PROCEDURE MASK (BLUE, YELLOW)
- K972883 — ISOSAFE EARLOOP PROCEDURE MASK (BLUE, YELLOW)
Adverse events under product code MDM
product code MDM- Injury
- 247
- Malfunction
- 1,516
- Total
- 1,763
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.