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FDA 510(k)

PMT DEPTHALON DEPTH #2102

K-Number: K802152 · 1980-11-19

Decision Date1980-11-19
Product CodeGZL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PMT DEPTHALON DEPTH #2102 is the device name listed in this FDA 510(k) record. The listed applicant is Progress Mankind Technology. It received FDA 510(k) clearance on 1980-11-19 under 510(k) number K802152. The device is classified under product code GZL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 17 devices →

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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