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FDA 510(k)

PROCHEK G GLUTARALDEHYDE CONCENTRATION LEVEL INDICATOR

K-Number: K960089 · 1996-04-04

Decision Date1996-04-04
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PROCHEK G GLUTARALDEHYDE CONCENTRATION LEVEL INDICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Cottrell, Ltd.. It received FDA 510(k) clearance on 1996-04-04 under 510(k) number K960089. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 9 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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