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FDA 510(k)

FILTER, BACTERIA (#2290)

K-Number: K760081 · 1976-07-15

ApplicantInspiron Corp.
Decision Date1976-07-15
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FILTER, BACTERIA (#2290) is the device name listed in this FDA 510(k) record. The listed applicant is Inspiron Corp.. It received FDA 510(k) clearance on 1976-07-15 under 510(k) number K760081. 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 FILTER, BACTERIA (#2290)?

FILTER, BACTERIA (#2290) is a medical device that received FDA 510(k) clearance on 1976-07-15. The listed applicant is Inspiron Corp.. The 510(k) number is K760081.

When did FILTER, BACTERIA (#2290) receive FDA 510(k) clearance?

FILTER, BACTERIA (#2290) received FDA 510(k) clearance on 1976-07-15, under 510(k) number K760081.

Who is the listed applicant for FILTER, BACTERIA (#2290)?

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

What is the FDA product code for FILTER, BACTERIA (#2290)?

The FDA product code for FILTER, BACTERIA (#2290) is 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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