510(k) K961791
K961791 is an FDA 510(k) premarket notification submitted by Depuy, Inc. for the device "DEPUY DISPOSABLE FILTER/HOOD". The FDA issued a decision of Substantially Equivalent on August 9, 1996. The device falls under product code LYU (Accessory, Surgical Apparel), a Class I device regulated under 21 CFR 878.4040. Depuy, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 9, 1996
- Date Received
- May 9, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Accessory, Surgical Apparel
- Device Class
- Class I
- Regulation Number
- 878.4040
- Review Panel
- HO
- Submission Type