510(k) K863820
K863820 is an FDA 510(k) premarket notification submitted by Gibco Laboratories Life Technologies, Inc. for the device "DRI-FORM: GBNA LISTERIA MEDIUM NO. M22300". The FDA issued a decision of Substantially Equivalent on Oct 8, 1986. The device falls under product code JSJ (Culture Media, Selective And Non-Differential), a Class I device regulated under 21 CFR 866.2360. Gibco Laboratories Life Technologies, Inc. has 66 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 8, 1986
- Date Received
- Sep 30, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Culture Media, Selective And Non-Differential
- Device Class
- Class I
- Regulation Number
- 866.2360
- Review Panel
- MI
- Submission Type
- 510(k) Exempt