FIELD MEDICAL OXYGEN GEN/DIST SYS-BATTLEFIELD PURP
K-Number: K903411 · 1990-08-31
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Device Summary
Frequently Asked Questions
What is the FIELD MEDICAL OXYGEN GEN/DIST SYS-BATTLEFIELD PURP?
FIELD MEDICAL OXYGEN GEN/DIST SYS-BATTLEFIELD PURP is a medical device that received FDA 510(k) clearance on 1990-08-31. The listed applicant is Guild Assoc., Inc.. The 510(k) number is K903411.
When did FIELD MEDICAL OXYGEN GEN/DIST SYS-BATTLEFIELD PURP receive FDA 510(k) clearance?
FIELD MEDICAL OXYGEN GEN/DIST SYS-BATTLEFIELD PURP received FDA 510(k) clearance on 1990-08-31, under 510(k) number K903411.
Who is the listed applicant for FIELD MEDICAL OXYGEN GEN/DIST SYS-BATTLEFIELD PURP?
The FDA 510(k) record lists Guild Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FIELD MEDICAL OXYGEN GEN/DIST SYS-BATTLEFIELD PURP?
The FDA product code for FIELD MEDICAL OXYGEN GEN/DIST SYS-BATTLEFIELD PURP is CAW.
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 Guild Assoc., 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: CAW)
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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