510(k) K831653
K831653 is an FDA 510(k) premarket notification submitted by Austin Biological Laboratories for the device "LYOPHILIZED MICROORGANISMS". The FDA issued a decision of Substantially Equivalent on July 28, 1983. The device falls under product code JTR (Kit, Quality Control For Culture Media), a Class I device regulated under 21 CFR 866.2480. Austin Biological Laboratories has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 28, 1983
- Date Received
- May 23, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Kit, Quality Control For Culture Media
- Device Class
- Class I
- Regulation Number
- 866.2480
- Review Panel
- MI
- Submission Type