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FDA 510(k)

HYDRO-BAC FILTER

K-Number: K852866 · 1986-01-01

ApplicantMedicomp, Inc.
Decision Date1986-01-01
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HYDRO-BAC FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Medicomp, Inc.. It received FDA 510(k) clearance on 1986-01-01 under 510(k) number K852866. The device is classified under product code CAI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYDRO-BAC FILTER?

HYDRO-BAC FILTER is a medical device that received FDA 510(k) clearance on 1986-01-01. The listed applicant is Medicomp, Inc.. The 510(k) number is K852866.

When did HYDRO-BAC FILTER receive FDA 510(k) clearance?

HYDRO-BAC FILTER received FDA 510(k) clearance on 1986-01-01, under 510(k) number K852866.

Who is the listed applicant for HYDRO-BAC FILTER?

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

What is the FDA product code for HYDRO-BAC FILTER?

The FDA product code for HYDRO-BAC FILTER is CAI.

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Related Devices (Code: CAI)

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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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