510(k) K964637
K964637 is an FDA 510(k) premarket notification submitted by Medical Packaging Corp. for the device "CULTURE COLLECTION AND TRANSPORT SYSTEM, MODIFIED AMIES MEDIA". The FDA issued a decision of Substantially Equivalent on December 24, 1996. The device falls under product code JSM (Culture Media, Non-Propagating Transport), a Class I device regulated under 21 CFR 866.2390. Medical Packaging Corp. has at least 9 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 24, 1996
- Date Received
- November 19, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Culture Media, Non-Propagating Transport
- Device Class
- Class I
- Regulation Number
- 866.2390
- Review Panel
- MI
- Submission Type