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FDA 510(k)

LICHEN, BACTERIAL IN LINE BREATHING FILTER

K-Number: K980662 · 1998-09-14

ApplicantDhd Healthcare Corp.
Decision Date1998-09-14
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LICHEN, BACTERIAL IN LINE BREATHING FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Dhd Healthcare Corp.. It received FDA 510(k) clearance on 1998-09-14 under 510(k) number K980662. 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 LICHEN, BACTERIAL IN LINE BREATHING FILTER?

LICHEN, BACTERIAL IN LINE BREATHING FILTER is a medical device that received FDA 510(k) clearance on 1998-09-14. The listed applicant is Dhd Healthcare Corp.. The 510(k) number is K980662.

When did LICHEN, BACTERIAL IN LINE BREATHING FILTER receive FDA 510(k) clearance?

LICHEN, BACTERIAL IN LINE BREATHING FILTER received FDA 510(k) clearance on 1998-09-14, under 510(k) number K980662.

Who is the listed applicant for LICHEN, BACTERIAL IN LINE BREATHING FILTER?

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

What is the FDA product code for LICHEN, BACTERIAL IN LINE BREATHING FILTER?

The FDA product code for LICHEN, BACTERIAL IN LINE BREATHING FILTER is CAH.

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Other records listing Dhd Healthcare Corp. as applicant

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Related Devices (Code: CAH)

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.

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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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