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FDA 510(k)

DRYDEN MINI BACTERIA FILTER

K-Number: K833066 · 1983-10-28

ApplicantDryden Corp.
Decision Date1983-10-28
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DRYDEN MINI BACTERIA FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Dryden Corp.. It received FDA 510(k) clearance on 1983-10-28 under 510(k) number K833066. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRYDEN MINI BACTERIA FILTER?

DRYDEN MINI BACTERIA FILTER is a medical device that received FDA 510(k) clearance on 1983-10-28. The listed applicant is Dryden Corp.. The 510(k) number is K833066.

When did DRYDEN MINI BACTERIA FILTER receive FDA 510(k) clearance?

DRYDEN MINI BACTERIA FILTER received FDA 510(k) clearance on 1983-10-28, under 510(k) number K833066.

Who is the listed applicant for DRYDEN MINI BACTERIA FILTER?

The FDA 510(k) record lists Dryden Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DRYDEN MINI BACTERIA FILTER?

The FDA product code for DRYDEN MINI BACTERIA FILTER is CAH.

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Related Devices (Code: CAH)

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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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