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FDA 510(k)

TORQUE FITTING

K-Number: K912969 · 1991-11-05

Decision Date1991-11-05
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TORQUE FITTING is the device name listed in this FDA 510(k) record. The listed applicant is Freedom Machine, Inc.. It received FDA 510(k) clearance on 1991-11-05 under 510(k) number K912969. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TORQUE FITTING?

TORQUE FITTING is a medical device that received FDA 510(k) clearance on 1991-11-05. The listed applicant is Freedom Machine, Inc.. The 510(k) number is K912969.

When did TORQUE FITTING receive FDA 510(k) clearance?

TORQUE FITTING received FDA 510(k) clearance on 1991-11-05, under 510(k) number K912969.

Who is the listed applicant for TORQUE FITTING?

The FDA 510(k) record lists Freedom Machine, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TORQUE FITTING?

The FDA product code for TORQUE FITTING is DTL.

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.

Related Devices (Code: DTL)

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

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