PROCHEK G GLUTARALDEHYDE CONCENTRATION LEVEL INDICATOR
K-Number: K960089 · 1996-04-04
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Device Summary
Frequently Asked Questions
What is the PROCHEK G GLUTARALDEHYDE CONCENTRATION LEVEL INDICATOR?
PROCHEK G GLUTARALDEHYDE CONCENTRATION LEVEL INDICATOR is a medical device that received FDA 510(k) clearance on 1996-04-04. The listed applicant is Cottrell, Ltd.. The 510(k) number is K960089.
When did PROCHEK G GLUTARALDEHYDE CONCENTRATION LEVEL INDICATOR receive FDA 510(k) clearance?
PROCHEK G GLUTARALDEHYDE CONCENTRATION LEVEL INDICATOR received FDA 510(k) clearance on 1996-04-04, under 510(k) number K960089.
Who is the listed applicant for PROCHEK G GLUTARALDEHYDE CONCENTRATION LEVEL INDICATOR?
The FDA 510(k) record lists Cottrell, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROCHEK G GLUTARALDEHYDE CONCENTRATION LEVEL INDICATOR?
The FDA product code for PROCHEK G GLUTARALDEHYDE CONCENTRATION LEVEL INDICATOR is JOJ.
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 Cottrell, Ltd. 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: JOJ)
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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