510(k) K925079
K925079 is an FDA 510(k) premarket notification submitted by Endo Technic Corp. for the device "LAPAROSCOPIC INST. (SCISSORS,FORCEPS,NEEDLEHOLDER)". The FDA issued a decision of Substantially Equivalent on August 24, 1994. The device falls under product code HET (Laparoscope, Gynecologic (And Accessories)), a Class II device regulated under 21 CFR 884.1720. Endo Technic Corp. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 24, 1994
- Date Received
- October 7, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Laparoscope, Gynecologic (And Accessories)
- Device Class
- Class II
- Regulation Number
- 884.1720
- Review Panel
- OB
- Submission Type