Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PMT TRACTION TONGS

K-Number: K871663 · 1987-06-19

Decision Date1987-06-19
Product CodeHAX
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PMT TRACTION TONGS 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 1987-06-19 under 510(k) number K871663. The device is classified under product code HAX. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PMT TRACTION TONGS?

PMT TRACTION TONGS is a medical device that received FDA 510(k) clearance on 1987-06-19. The listed applicant is Progress Mankind Technology. The 510(k) number is K871663.

When did PMT TRACTION TONGS receive FDA 510(k) clearance?

PMT TRACTION TONGS received FDA 510(k) clearance on 1987-06-19, under 510(k) number K871663.

Who is the listed applicant for PMT TRACTION TONGS?

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 TRACTION TONGS?

The FDA product code for PMT TRACTION TONGS is HAX.

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: HAX)

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.

↑