ANESTHESIA RESPIRATORY BREATH CIRCUIT PACKS/COMPON
K-Number: K926454 · 1993-06-22
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Device Summary
Frequently Asked Questions
What is the ANESTHESIA RESPIRATORY BREATH CIRCUIT PACKS/COMPON?
ANESTHESIA RESPIRATORY BREATH CIRCUIT PACKS/COMPON is a medical device that received FDA 510(k) clearance on 1993-06-22. The listed applicant is Medical, Inc.. The 510(k) number is K926454.
When did ANESTHESIA RESPIRATORY BREATH CIRCUIT PACKS/COMPON receive FDA 510(k) clearance?
ANESTHESIA RESPIRATORY BREATH CIRCUIT PACKS/COMPON received FDA 510(k) clearance on 1993-06-22, under 510(k) number K926454.
Who is the listed applicant for ANESTHESIA RESPIRATORY BREATH CIRCUIT PACKS/COMPON?
The FDA 510(k) record lists Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANESTHESIA RESPIRATORY BREATH CIRCUIT PACKS/COMPON?
The FDA product code for ANESTHESIA RESPIRATORY BREATH CIRCUIT PACKS/COMPON 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 Medical, 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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