TRI PAC MOUTH PROP
K-Number: K800369 · 1980-02-28
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Device Summary
Frequently Asked Questions
What is the TRI PAC MOUTH PROP?
TRI PAC MOUTH PROP is a medical device that received FDA 510(k) clearance on 1980-02-28. The listed applicant is Oxequip Health Ind.. The 510(k) number is K800369.
When did TRI PAC MOUTH PROP receive FDA 510(k) clearance?
TRI PAC MOUTH PROP received FDA 510(k) clearance on 1980-02-28, under 510(k) number K800369.
Who is the listed applicant for TRI PAC MOUTH PROP?
The FDA 510(k) record lists Oxequip Health Ind. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRI PAC MOUTH PROP?
The FDA product code for TRI PAC MOUTH PROP is JXL.
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 Oxequip Health Ind. 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: JXL)
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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