K993123Substantially Equivalent
Qk-Wide Band Spectrum Therapeutic Apparatus, Models Co1a, Co1b, Co1c, Co1d, Co2a, Co2b
united pacific Company, Alhambra CA / Traditional, Substantially Equivalent
K993123 is the FDA 510(k) clearance record for QK-WIDE BAND SPECTRUM THERAPEUTIC APPARATUS, MODELS CO1A, CO1B, CO1C, CO1D, CO2A, CO2B, a class II device, cleared for United Pacific Co., Ltd. on under FDA product code ILY (Lamp, Infrared, Therapeutic Heating). FDA records list 6 510(k) clearances for United Pacific Co., Ltd., from to . As of , FDA records show no recalls naming K993123.
Clearance record
- Decision date
- Received
- (88 days to decision)
- Product code
- ILY Lamp, Infrared, Therapeutic Heating
- Regulation
- 21 CFR 890.5500
- Device class
- Class II
- Review panel
- Physical Medicine
- Applicant
- United Pacific Co., Ltd. 219 S. Raymond Ave., Alhambra CA
- 510(k) summary
- Statement
- Third party review
- No
Clearances, product code ILY
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 1 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
