Insta-Flo
by Medtec LLC
510(k) K935209
Insta-Flo is a medical device (FDA Class II; FDA product code JAD, System, Therapeutic, X-Ray) made by Medtec LLC, cleared under FDA 510(k) K935209 on 13 Dec 1993, active as of 11 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK935209 | Date13 Dec 1993 | StatusActive |
Official records
- FDA 510(k) database K935209
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- JAD
- FDA applicant
- Medtec, Inc.
- Device class
- Class II
- Regulation
- 21 CFR Part 892.5900
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
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