ISOSAFE EARLOOP PROCEDURE MASK (BLUE, YELLOW)— 510(k) K972849
Substantially EquivalentCypress Medical Products, Ltd.
FDA 510(k) clearance K972849 for ISOSAFE EARLOOP PROCEDURE MASK (BLUE, YELLOW), Substantially Equivalent on 1998-05-28. Applicant: Cypress Medical Products, Ltd.. Device class: 2.
Clearance details
- Applicant
- Cypress Medical Products, Ltd.
- Product code
- Code FXX
- Device class
- Class 2
- Regulation
- 21 CFR 878.4040
- 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 FXX
view all- K251967 — HALYARD* FLUIDSHIELD* 3 Fog-Free Procedure Mask with SO SOFT* Lining and SO SOFT* Earloops +1 more
- K252534 — Surgical Face Mask (Ear mount)
- K253398 — Disposable Surgical Mask (Non-Sterile) (EFX3PLBLKMSK300)
- K252830 — Disposable Surgical Face Mask (3P00B, C2900)
- K252650 — Disposable Medical Face Mask
More 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
- K972883 — ISOSAFE EARLOOP PROCEDURE MASK (BLUE, YELLOW)
- K952367 — CYPRESS MEDICAL PRODUCTS VINYL EXAMINATION GLOVE
Adverse events under product code FXX
product code FXX- Injury
- 137
- Total
- 137
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.