FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
X-RAY CO-ORDINATOR
K Number: K772313
·
Decision Jan 30, 1978
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
9
Applicant Total
5
Review Days
49
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Basic Information
- Device Name
- X-RAY CO-ORDINATOR
- K Number
- K772313
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 892.1920
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Applicant
- Rinn Corp.
- Date Received
- December 12, 1977
- Decision Date
- January 30, 1978
- Product Code
- IWY
- Advisory Committee
- Radiology
- Review Advisory Committee
- RA
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| IWY | Holder, Head, Radiographic | FDA class 1 | Radiology |
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Other Clearances by Rinn Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K932134 | RINN UNIVERSAL COLLIMATOR | Jul 26, 1993 | Substantially Equivalent |
| K913885 | RINN E-Z CAPPER | Dec 13, 1991 | Substantially Equivalent |
| K828605 | BEAM LIMITING DEVICE | Jan 3, 1983 | Substantially Equivalent |
| K813378 | UNI-BITE DENTAL X-RAY FILM HOLDER | Jan 29, 1982 | Substantially Equivalent |