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FDA 510(k)

R1618, R1619 & R1654 ICE MAKING MACHINES

K-Number: K861343 · 1986-07-17

ApplicantTri W-G, Inc.
Decision Date1986-07-17
Product Code
DecisionSubstantially Equivalent

Device Summary

R1618, R1619 & R1654 ICE MAKING MACHINES is the device name listed in this FDA 510(k) record. The listed applicant is Tri W-G, Inc.. It received FDA 510(k) clearance on 1986-07-17 under 510(k) number K861343. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the R1618, R1619 & R1654 ICE MAKING MACHINES?

R1618, R1619 & R1654 ICE MAKING MACHINES is a medical device that received FDA 510(k) clearance on 1986-07-17. The listed applicant is Tri W-G, Inc.. The 510(k) number is K861343.

When did R1618, R1619 & R1654 ICE MAKING MACHINES receive FDA 510(k) clearance?

R1618, R1619 & R1654 ICE MAKING MACHINES received FDA 510(k) clearance on 1986-07-17, under 510(k) number K861343.

Who is the listed applicant for R1618, R1619 & R1654 ICE MAKING MACHINES?

The FDA 510(k) record lists Tri W-G, Inc. as the applicant. This does not by itself establish the device manufacturer.

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 Tri W-G, Inc. 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.

K960196TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777K945163ECHOCARDIOGRAPHYK941720MODEL 747 AND 747-30 EXAM/TREATMENT TABLEK936303TREATMENT TABLE MODIFICATIONK933119HI-LO TREATMENT TABLESK932746MODEL T4501,T4502,T4503,T4504,T4504 TILT TABLE

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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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