HI-M-TEST MORPHINE
K-Number: K791551 · 1979-10-17
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Device Summary
Frequently Asked Questions
What is the HI-M-TEST MORPHINE?
HI-M-TEST MORPHINE is a medical device that received FDA 510(k) clearance on 1979-10-17. The listed applicant is Technam, Inc.. The 510(k) number is K791551.
When did HI-M-TEST MORPHINE receive FDA 510(k) clearance?
HI-M-TEST MORPHINE received FDA 510(k) clearance on 1979-10-17, under 510(k) number K791551.
Who is the listed applicant for HI-M-TEST MORPHINE?
The FDA 510(k) record lists Technam, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HI-M-TEST MORPHINE?
The FDA product code for HI-M-TEST MORPHINE is DLR.
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 Technam, 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: DLR)
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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