Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DISPOSABLE BACTERIAL BREATHNG FILTER

K-Number: K915750 · 1994-11-30

Decision Date1994-11-30
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE BACTERIAL BREATHNG FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Hospitak, Inc.. It received FDA 510(k) clearance on 1994-11-30 under 510(k) number K915750. 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 DISPOSABLE BACTERIAL BREATHNG FILTER?

DISPOSABLE BACTERIAL BREATHNG FILTER is a medical device that received FDA 510(k) clearance on 1994-11-30. The listed applicant is Hospitak, Inc.. The 510(k) number is K915750.

When did DISPOSABLE BACTERIAL BREATHNG FILTER receive FDA 510(k) clearance?

DISPOSABLE BACTERIAL BREATHNG FILTER received FDA 510(k) clearance on 1994-11-30, under 510(k) number K915750.

Who is the listed applicant for DISPOSABLE BACTERIAL BREATHNG FILTER?

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

What is the FDA product code for DISPOSABLE BACTERIAL BREATHNG FILTER?

The FDA product code for DISPOSABLE BACTERIAL BREATHNG FILTER is CAH.

Related Clinical Trials

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.

Other records listing Hospitak, Inc. as applicant

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.

View all 27 devices →

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.

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.

↑