K930220Substantially Equivalent
Cassette, Radiographic Film
X-Ray Accessories Mfg. Co., Putnam CT / Traditional, Substantially Equivalent
K930220 is the FDA 510(k) clearance record for CASSETTE, RADIOGRAPHIC FILM, a class II device, cleared for X-Ray Accessories Mfg. Co. on under FDA product code IXA (Cassette, Radiographic Film). FDA records list 2 510(k) clearances for X-Ray Accessories Mfg. Co., from to . As of , FDA records show no recalls naming K930220.
Clearance record
- Decision date
- Received
- (88 days to decision)
- Product code
- IXA Cassette, Radiographic Film
- Regulation
- 21 CFR 892.1850
- Device class
- Class II
- Review panel
- Radiology
- Applicant
- X-Ray Accessories Mfg. Co. 5 Canal St., Putnam CT
- 510(k) summary
- Statement
- Third party review
- No
Clearances, product code IXA
Trailing 12 monthsFDA records hold no clearances under product code IXA in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| 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.
