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FDA 510(k)

TRANSTUBE MW176 OT MD176

K-Number: K872213 · 1987-06-23

ApplicantMedical Wire & Equipment Co.
Decision Date1987-06-23
Product CodeJSM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TRANSTUBE MW176 OT MD176 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Wire & Equipment Co.. It received FDA 510(k) clearance on 1987-06-23 under 510(k) number K872213. The device is classified under product code JSM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSTUBE MW176 OT MD176?

TRANSTUBE MW176 OT MD176 is a medical device that received FDA 510(k) clearance on 1987-06-23. The listed applicant is Medical Wire & Equipment Co.. The 510(k) number is K872213.

When did TRANSTUBE MW176 OT MD176 receive FDA 510(k) clearance?

TRANSTUBE MW176 OT MD176 received FDA 510(k) clearance on 1987-06-23, under 510(k) number K872213.

Who is the listed applicant for TRANSTUBE MW176 OT MD176?

The FDA 510(k) record lists Medical Wire & Equipment Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRANSTUBE MW176 OT MD176?

The FDA product code for TRANSTUBE MW176 OT MD176 is JSM.

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.

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Other records listing Medical Wire & Equipment Co. 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.

K900112MICRORING YT

Related Devices (Code: JSM)

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.

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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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