510(k) K923176
K923176 is an FDA 510(k) premarket notification submitted by Ulti-Med Intl., Inc. for the device "SURGICAL INSTRUMENT KIT, DISPOSABLE". The FDA issued a decision of Substantially Equivalent on June 17, 1993. The device falls under product code KDD (Kit, Surgical Instrument, Disposable), a Class I device regulated under 21 CFR 878.4800. Ulti-Med Intl., Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 17, 1993
- Date Received
- June 12, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Kit, Surgical Instrument, Disposable
- Device Class
- Class I
- Regulation Number
- 878.4800
- Review Panel
- SU
- Submission Type