PARAMAX ALCOHOL AND AMMONIA CALIBRATOR, I & II
K-Number: K881258 · 1988-05-27
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Device Summary
Frequently Asked Questions
What is the PARAMAX ALCOHOL AND AMMONIA CALIBRATOR, I & II?
PARAMAX ALCOHOL AND AMMONIA CALIBRATOR, I & II is a medical device that received FDA 510(k) clearance on 1988-05-27. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K881258.
When did PARAMAX ALCOHOL AND AMMONIA CALIBRATOR, I & II receive FDA 510(k) clearance?
PARAMAX ALCOHOL AND AMMONIA CALIBRATOR, I & II received FDA 510(k) clearance on 1988-05-27, under 510(k) number K881258.
Who is the listed applicant for PARAMAX ALCOHOL AND AMMONIA CALIBRATOR, I & II?
The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PARAMAX ALCOHOL AND AMMONIA CALIBRATOR, I & II?
The FDA product code for PARAMAX ALCOHOL AND AMMONIA CALIBRATOR, I & II is JIX.
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 Healthcare Corp 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: JIX)
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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