# Cypress Medical Products, Ltd.

- Location (FDA's records): Mc Henry, IL
- FDA decisions: 26 (1989–2002): 26 510(k) clearances
- Product codes: LYZ (3), LYY (3), EFQ (2), FCM (2), FXX (2), LRO (2), GDT (1), HIB (1), FRG (1), KKX (1), MDM (1), EYZ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K021676: Cypress Medical Products, LP Disposable Vaginal Speculum, Non-Metal (Jul 12, 2002)
- K012282: Sterile Powder Free Synthetic Vinyl Patient Exam Glove (Aug 6, 2001)
- K972899: Cypress Medical Products Aneroid Sphygmomanometer (Jul 7, 1998)
- K972849: Isosafe Earloop Procedure Mask (Blue, Yellow) (May 28, 1998)
- K972883: Isosafe Earloop Procedure Mask (Blue, Yellow) (Feb 26, 1998)
- K952367: Cypress Medical Products Vinyl Examination Glove (Jul 5, 1995)
- K950254: Cypress Medical Products Sterile Latex Examination Glove (Mar 31, 1995)
- K950109: Cypress Medical Products Catheter (Insertion) Tray/with Out Catheter (Feb 27, 1995)

Source page: https://510kreport.com/company/cypress-medical-products