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FDA 510(k)

DAILY WASH SOLUTION 5

K-Number: K841421 · 1984-05-11

Decision Date1984-05-11
Product CodeJJO
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DAILY WASH SOLUTION 5 is the device name listed in this FDA 510(k) record. The listed applicant is Reagent Laboratory, Inc.. It received FDA 510(k) clearance on 1984-05-11 under 510(k) number K841421. The device is classified under product code JJO. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAILY WASH SOLUTION 5?

DAILY WASH SOLUTION 5 is a medical device that received FDA 510(k) clearance on 1984-05-11. The listed applicant is Reagent Laboratory, Inc.. The 510(k) number is K841421.

When did DAILY WASH SOLUTION 5 receive FDA 510(k) clearance?

DAILY WASH SOLUTION 5 received FDA 510(k) clearance on 1984-05-11, under 510(k) number K841421.

Who is the listed applicant for DAILY WASH SOLUTION 5?

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

What is the FDA product code for DAILY WASH SOLUTION 5?

The FDA product code for DAILY WASH SOLUTION 5 is JJO.

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 Reagent Laboratory, 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 19 devices →

Related Devices (Code: JJO)

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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