510(k) K902552
K902552 is an FDA 510(k) premarket notification submitted by Gerber Products Co. for the device "GERBER PRECIOUS CARE ELECTRIC BREAST PUMP". The FDA issued a decision of Substantially Equivalent on September 26, 1990. The device falls under product code HGY (Pump, Breast, Non-Powered), a Class I device regulated under 21 CFR 884.5150. Gerber Products Co. has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 26, 1990
- Date Received
- June 8, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Pump, Breast, Non-Powered
- Device Class
- Class I
- Regulation Number
- 884.5150
- Review Panel
- OB
- Submission Type