510(k) K894413
K894413 is an FDA 510(k) premarket notification submitted by Inmark Corp. for the device "X-RAY TUBE HOUSING ASSEMBLY, VARIOUS MODELS". The FDA issued a decision of Substantially Equivalent on September 22, 1989. The device falls under product code ITY (Assembly, Tube Housing, X-Ray, Diagnostic), a Class I device regulated under 21 CFR 892.1760. Inmark Corp. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 22, 1989
- Date Received
- July 17, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Assembly, Tube Housing, X-Ray, Diagnostic
- Device Class
- Class I
- Regulation Number
- 892.1760
- Review Panel
- RA
- Submission Type