MARTIN-LEWIS AGAR MEDIUM— 510(k) K770287
Substantially EquivalentGibco Laboratories Life Technologies, Inc.
FDA 510(k) clearance K770287 for MARTIN-LEWIS AGAR MEDIUM, Substantially Equivalent on 1977-02-18. Applicant: Gibco Laboratories Life Technologies, Inc.. Device class: 2.
Clearance details
- Applicant
- Gibco Laboratories Life Technologies, Inc.
- Product code
- Code JTY
- Device class
- Class 2
- Regulation
- 21 CFR 866.2410
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code JTY
view allMore clearances from Gibco Laboratories Life Technologies, Inc.
view allRecalls naming K770287
K-number listed on FDA's recall record- Z-1377-2021 — BD BBL Martin-Lewis Agar, 100 Ea - Product Usage: used for the isolation of pathogenic Neisseria from specimens containing mixed flora of bacteria and fungi. Catalog Number: 221558
- Z-1378-2021 — BD BBL Martin-Lewis Agar 20 Ea - Product Usage: use for the isolation of pathogenic Neisseria from specimens containing mixed flora of bacteria and fungi. Catalog Number: 221557
Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K770287.
Data sourced from openFDA. This site is unofficial and independent of the FDA.