Barrierplus Synthetic Powder-Free Surgical Gloves
K990710 is the FDA 510(k) clearance record for BARRIERPLUS SYNTHETIC POWDER-FREE SURGICAL GLOVES, a class I device, cleared for Barriermed Glove Co. on under FDA product code KGO (Surgeon'S Gloves). FDA's definition for product code KGO reads: "A surgeon's glove is a disposable device made of natural rubber latex or synthetic polymers that may or may not bear powder to facilitate donning, and it is intended to be worn on the hands, usually in surgical settings, to provide a...". FDA records list 5 510(k) clearances for Barriermed Glove Co., from to . As of , FDA records show no recalls naming K990710.
Clearance record
- Decision date
- Received
- (77 days to decision)
- Product code
- KGO Surgeon'S Gloves
- Regulation
- 21 CFR 878.4460
- Device class
- Class I
- Review panel
- General, Plastic Surgery
- Applicant
- Barriermed Glove Co. 2500 W. Lake Mary Blvd., Lake Mary FL
- 510(k) summary
- Statement
- Third party review
- No
Clearances, product code KGO
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 1 |
| June 2026 | 0 |
| July 2026 | 1 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
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