PMT DEPTHALON DEPTH #2102
K-Number: K802152 · 1980-11-19
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Device Summary
Frequently Asked Questions
What is the PMT DEPTHALON DEPTH #2102?
PMT DEPTHALON DEPTH #2102 is a medical device that received FDA 510(k) clearance on 1980-11-19. The listed applicant is Progress Mankind Technology. The 510(k) number is K802152.
When did PMT DEPTHALON DEPTH #2102 receive FDA 510(k) clearance?
PMT DEPTHALON DEPTH #2102 received FDA 510(k) clearance on 1980-11-19, under 510(k) number K802152.
Who is the listed applicant for PMT DEPTHALON DEPTH #2102?
The FDA 510(k) record lists Progress Mankind Technology as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PMT DEPTHALON DEPTH #2102?
The FDA product code for PMT DEPTHALON DEPTH #2102 is GZL.
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 Progress Mankind Technology 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: GZL)
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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