510(k) K791557
K791557 is an FDA 510(k) premarket notification submitted by American Laboratory Supply, Inc. for the device "MARTIN-LEWIS AGAR (PLATE)". The FDA issued a decision of Substantially Equivalent on Sep 17, 1979. The device falls under product code JTY (Culture Media, For Isolation Of Pathogenic Neisseria), a Class II device regulated under 21 CFR 866.2410. American Laboratory Supply, Inc. has 35 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Sep 17, 1979
- Date Received
- Aug 17, 1979
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Culture Media, For Isolation Of Pathogenic Neisseria
- Device Class
- Class II
- Regulation Number
- 866.2410
- Review Panel
- MI
- Submission Type
- 510(k)