Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Britt Corp., Inc. — Predicate Candidate Screening
17 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
122 daysmedian FDA review time
451 days90th percentile
17clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K003828 | VASO PRESS DVT FOOT GARMENT #VP 520 | Britt Corp., Inc. | 2001-05-18 | 158 | 0 |
| K991038 | VASO PRESS DVT SYSTEM, MODELS VP500, VP501 | Britt Corp., Inc. | 2000-06-22 | 451 | 0 |
| K974393 | VASO PRESS SYSTEM | Britt Corp., Inc. | 1999-03-19 | 483 | 0 |
| K860977 | MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATION | Britt Corp., Inc. | 1986-10-16 | 216 | 0 |
| K860975 | MODEL 545-45 LASER FOR EAR, NOSE & THROAT | Britt Corp., Inc. | 1986-07-18 | 126 | 0 |
| K860974 | MODEL 545-45 LASER FOR DERMA., POD., SURGICAL | Britt Corp., Inc. | 1986-07-07 | 115 | 0 |
| K860277 | MODEL 525-25 WATT C02 LASER FOR EAR, NOSE & THROAT | Britt Corp., Inc. | 1986-05-06 | 99 | 0 |
| K860273 | MODEL 525 - 25 WATT CO2 MEDICAL LASER/PODIATRY | Britt Corp., Inc. | 1986-04-23 | 86 | 0 |
| K860278 | MODEL 525-25 WATT CO2 LASER FOR DERMA/PLASTIC | Britt Corp., Inc. | 1986-04-15 | 78 | 0 |
| K851425 | MODEL J25-25 WATT CO2 LASER | Britt Corp., Inc. | 1985-11-12 | 216 | 0 |
| K840036 | FITEX | Britt Corp., Inc. | 1984-10-26 | 295 | 0 |
| K840020 | FITNESS LOGGER | Britt Corp., Inc. | 1984-10-26 | 295 | 0 |
| K833533 | LASER PHOTOCOAGULATOR 1520-A & K | Britt Corp., Inc. | 1984-01-30 | 111 | 0 |
| K837200 | BRITT SURGICAL PHOTOCOAGULATOR SYSTEM | Britt Corp., Inc. | 1983-04-04 | 70 | 0 |
| K837151 | BLUE GREEN FILTER SYSTEM TO MODEL 152 AND 150 LASER SYSTEM | Britt Corp., Inc. | 1983-03-22 | 57 | 0 |
| K813492 | BRITT KRYPTON LASERS 150K & 152K | Britt Corp., Inc. | 1982-01-22 | 42 | 0 |
| K790694 | BRITT LENS COMPUTER | Britt Corp., Inc. | 1979-08-10 | 122 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda