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FDA 510(k)

PRO-PACT PERACETIC ACID CULTURE TEST KIT, MODEL C-3PA

K-Number: K031114 · 2004-03-03

Decision Date2004-03-03
Product CodeMRB
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PRO-PACT PERACETIC ACID CULTURE TEST KIT, MODEL C-3PA is the device name listed in this FDA 510(k) record. The listed applicant is Raven Biological Laboratories, Inc.. It received FDA 510(k) clearance on 2004-03-03 under 510(k) number K031114. The device is classified under product code MRB. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRO-PACT PERACETIC ACID CULTURE TEST KIT, MODEL C-3PA?

PRO-PACT PERACETIC ACID CULTURE TEST KIT, MODEL C-3PA is a medical device that received FDA 510(k) clearance on 2004-03-03. The listed applicant is Raven Biological Laboratories, Inc.. The 510(k) number is K031114.

When did PRO-PACT PERACETIC ACID CULTURE TEST KIT, MODEL C-3PA receive FDA 510(k) clearance?

PRO-PACT PERACETIC ACID CULTURE TEST KIT, MODEL C-3PA received FDA 510(k) clearance on 2004-03-03, under 510(k) number K031114.

Who is the listed applicant for PRO-PACT PERACETIC ACID CULTURE TEST KIT, MODEL C-3PA?

The FDA 510(k) record lists Raven Biological Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PRO-PACT PERACETIC ACID CULTURE TEST KIT, MODEL C-3PA?

The FDA product code for PRO-PACT PERACETIC ACID CULTURE TEST KIT, MODEL C-3PA is MRB.

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 Raven Biological Laboratories, 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.

View all 15 devices →

Related Devices (Code: MRB)

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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