NICHOLAS II, VIRAL-BACTERIAL FILTER
K-Number: K811546 · 1981-08-03
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Device Summary
Frequently Asked Questions
What is the NICHOLAS II, VIRAL-BACTERIAL FILTER?
NICHOLAS II, VIRAL-BACTERIAL FILTER is a medical device that received FDA 510(k) clearance on 1981-08-03. The listed applicant is K & G Healthcare Ind., Inc.. The 510(k) number is K811546.
When did NICHOLAS II, VIRAL-BACTERIAL FILTER receive FDA 510(k) clearance?
NICHOLAS II, VIRAL-BACTERIAL FILTER received FDA 510(k) clearance on 1981-08-03, under 510(k) number K811546.
Who is the listed applicant for NICHOLAS II, VIRAL-BACTERIAL FILTER?
The FDA 510(k) record lists K & G Healthcare Ind., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NICHOLAS II, VIRAL-BACTERIAL FILTER?
The FDA product code for NICHOLAS II, VIRAL-BACTERIAL 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 K & G Healthcare Ind., 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.
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.
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