BREATHING CIRCUIT PRODUCTS, ANESTHESIA
K-Number: K781908 · 1978-11-27
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Device Summary
Frequently Asked Questions
What is the BREATHING CIRCUIT PRODUCTS, ANESTHESIA?
BREATHING CIRCUIT PRODUCTS, ANESTHESIA is a medical device that received FDA 510(k) clearance on 1978-11-27. The listed applicant is Hospitak, Inc.. The 510(k) number is K781908.
When did BREATHING CIRCUIT PRODUCTS, ANESTHESIA receive FDA 510(k) clearance?
BREATHING CIRCUIT PRODUCTS, ANESTHESIA received FDA 510(k) clearance on 1978-11-27, under 510(k) number K781908.
Who is the listed applicant for BREATHING CIRCUIT PRODUCTS, ANESTHESIA?
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 BREATHING CIRCUIT PRODUCTS, ANESTHESIA?
The FDA product code for BREATHING CIRCUIT PRODUCTS, ANESTHESIA is CAI.
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.
Related Devices (Code: CAI)
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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