MICRODILUTION/LORACARBEF PANELS
K-Number: K942089 · 1995-01-09
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Device Summary
Frequently Asked Questions
What is the MICRODILUTION/LORACARBEF PANELS?
MICRODILUTION/LORACARBEF PANELS is a medical device that received FDA 510(k) clearance on 1995-01-09. The listed applicant is Baxter Diagnostics, Inc.. The 510(k) number is K942089.
When did MICRODILUTION/LORACARBEF PANELS receive FDA 510(k) clearance?
MICRODILUTION/LORACARBEF PANELS received FDA 510(k) clearance on 1995-01-09, under 510(k) number K942089.
Who is the listed applicant for MICRODILUTION/LORACARBEF PANELS?
The FDA 510(k) record lists Baxter Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICRODILUTION/LORACARBEF PANELS?
The FDA product code for MICRODILUTION/LORACARBEF PANELS is JWY.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Baxter Diagnostics, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: JWY)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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