510(k) K970988
K970988 is an FDA 510(k) premarket notification submitted by Far East Science & Technology Development Co., Ltd. for the device "FAR-EAST BOUFFANT CAPS". The FDA issued a decision of Substantially Equivalent on July 10, 1997. The device falls under product code LYU (Accessory, Surgical Apparel), a Class I device regulated under 21 CFR 878.4040. Far East Science & Technology Development Co., Ltd. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 10, 1997
- Date Received
- March 18, 1997
- 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