510(k) K873272
K873272 is an FDA 510(k) premarket notification submitted by Stierlen-Maquet AG for the device "ENDOSCOPY TABLE 1532 ENDOSTAR". The FDA issued a decision of Substantially Equivalent on September 8, 1987. The device falls under product code BWN (Table And Attachments, Operating-Room), a Class I device regulated under 21 CFR 878.4950. Stierlen-Maquet AG has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 8, 1987
- Date Received
- August 17, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Table And Attachments, Operating-Room
- Device Class
- Class I
- Regulation Number
- 878.4950
- Review Panel
- SU
- Submission Type