Tempa-Kuff Single Pat Pre-Gaged Balanced Disp Cuff
by Pymah Corp. 510(k)
Active
510(k) K925744
Overview
This device is a blood pressure cuff classified under product code DXQ. It is a single-patient, pre-gaged, balanced disposable cuff designed for blood pressure measurement.
It is supplied as a sterile, single-use device. The device received FDA 510(k) clearance K925744 on July 30, 1993, and is classified as Class II with special controls.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK925744 | Date30 Jul 1993 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — FDA 510(k) Active
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- 510(k) Number
- FDA Product Code
- DXQ
- Device Class
- Class II
- Regulation
- 21 CFR Part 870.1120
- Advisory Committee
- Cardiovascular
- FDA Decision
- SESE Substantially Equivalent
Other devices from Pymah Corp.
Questions
What is the TEMPA-KUFF cuff used for?
The TEMPA-KUFF cuff is designed for blood pressure measurement as a single-patient, pre-gaged, balanced disposable device, intended for one-time use on one patient to prevent cross-contamination.
How is the TEMPA-KUFF cuff supplied and is it sterile?
The device is supplied as a sterile, single-use cuff, meaning it is sterilized before packaging and intended for one application only, after which it should be discarded to maintain infection control standards.
What regulatory clearance does the TEMPA-KUFF cuff have?
The TEMPA-KUFF cuff received FDA 510(k) clearance under number K925744 on July 30, 1993, and is classified as a Class II medical device with special controls under product code DXQ for blood pressure cuffs.