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FDA 510(k)

DRYDEN BACTERIA FILTER

K-Number: K792097 · 1979-11-13

ApplicantDryden Corp.
Decision Date1979-11-13
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DRYDEN 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 1979-11-13 under 510(k) number K792097. 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 BACTERIA FILTER?

DRYDEN BACTERIA FILTER is a medical device that received FDA 510(k) clearance on 1979-11-13. The listed applicant is Dryden Corp.. The 510(k) number is K792097.

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

DRYDEN BACTERIA FILTER received FDA 510(k) clearance on 1979-11-13, under 510(k) number K792097.

Who is the listed applicant for DRYDEN 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 BACTERIA FILTER?

The FDA product code for DRYDEN BACTERIA FILTER is CAH.

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Other records listing Dryden Corp. as applicant

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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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