K970992Substantially Equivalent
Premier Nitrospray Plus and Premier Nitrospray Lite Plus
Premier Dental Products Co, King Of Prussia PA / Traditional, Substantially Equivalent
K970992 is the FDA 510(k) clearance record for PREMIER NITROSPRAY PLUS AND PREMIER NITROSPRAY LITE PLUS, a class II device, cleared for Premier Dental Products Co. on under FDA product code GEH (Unit, Cryosurgical, Accessories). FDA records list 44 510(k) clearances for Premier Dental Products Co., from to . As of , FDA records show 2 recalls naming K970992.
Clearance record
- Decision date
- Received
- (90 days to decision)
- Product code
- GEH Unit, Cryosurgical, Accessories
- Regulation
- 21 CFR 878.4350
- Device class
- Class II
- Review panel
- General, Plastic Surgery
- Applicant
- Premier Dental Products Co. 3600 Horizon Dr., King Of Prussia PA
- 510(k) summary
- Summary
- Third party review
- No
Clearances, product code GEH
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 1 |
| January 2026 | 1 |
| February 2026 | 2 |
| March 2026 | 0 |
| April 2026 | 2 |
| May 2026 | 0 |
| June 2026 | 2 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 1 |
| 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.
