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FDA 510(k)

YOKE ASSEMBLY MEDICAL GAS

K-Number: K935283 · 1994-03-11

Decision Date1994-03-11
Product CodeCAM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

YOKE ASSEMBLY MEDICAL GAS is the device name listed in this FDA 510(k) record. The listed applicant is American Gage & Medical, Inc.. It received FDA 510(k) clearance on 1994-03-11 under 510(k) number K935283. The device is classified under product code CAM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YOKE ASSEMBLY MEDICAL GAS?

YOKE ASSEMBLY MEDICAL GAS is a medical device that received FDA 510(k) clearance on 1994-03-11. The listed applicant is American Gage & Medical, Inc.. The 510(k) number is K935283.

When did YOKE ASSEMBLY MEDICAL GAS receive FDA 510(k) clearance?

YOKE ASSEMBLY MEDICAL GAS received FDA 510(k) clearance on 1994-03-11, under 510(k) number K935283.

Who is the listed applicant for YOKE ASSEMBLY MEDICAL GAS?

The FDA 510(k) record lists American Gage & Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for YOKE ASSEMBLY MEDICAL GAS?

The FDA product code for YOKE ASSEMBLY MEDICAL GAS is CAM.

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: CAM)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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