SUTURE REMOVAL KIT— 510(k) K890729
Substantially EquivalentCypress Medical Products, Ltd.
FDA 510(k) clearance K890729 for SUTURE REMOVAL KIT, Substantially Equivalent on 1989-04-17. Applicant: Cypress Medical Products, Ltd.. Device class: 2.
Clearance details
- Applicant
- Cypress Medical Products, Ltd.
- Product code
- Code LRO
- Device class
- Class 2
- Regulation
- 21 CFR 878.4370
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mc Henry, IL, US
Recent devices under product code LRO
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 LRO
product code LRO- Injury
- 975
- Malfunction
- 14,038
- Other
- 2
- Total
- 15,015
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.