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FDA 510(k)

R1436,R1697,R1699,R1564,R1216,R1214,R854 & R1213

K-Number: K861350 · 1986-05-02

ApplicantTri W-G, Inc.
Decision Date1986-05-02
Product CodeINW
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

R1436,R1697,R1699,R1564,R1216,R1214,R854 & R1213 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 1986-05-02 under 510(k) number K861350. The device is classified under product code INW. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the R1436,R1697,R1699,R1564,R1216,R1214,R854 & R1213?

R1436,R1697,R1699,R1564,R1216,R1214,R854 & R1213 is a medical device that received FDA 510(k) clearance on 1986-05-02. The listed applicant is Tri W-G, Inc.. The 510(k) number is K861350.

When did R1436,R1697,R1699,R1564,R1216,R1214,R854 & R1213 receive FDA 510(k) clearance?

R1436,R1697,R1699,R1564,R1216,R1214,R854 & R1213 received FDA 510(k) clearance on 1986-05-02, under 510(k) number K861350.

Who is the listed applicant for R1436,R1697,R1699,R1564,R1216,R1214,R854 & R1213?

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

What is the FDA product code for R1436,R1697,R1699,R1564,R1216,R1214,R854 & R1213?

The FDA product code for R1436,R1697,R1699,R1564,R1216,R1214,R854 & R1213 is INW.

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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Related Devices (Code: INW)

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.

K944308JAMES LECKEY FREE STANDERJames Leckey DesignK944307JAMES LECKEY PRONE STANDERJames Leckey DesignK943974EURO TECH MARQUISE CHIROPRACTIC TABLEProgressive Electrical TherapeuticsK943975EURO TECH PLATINUM CHIROPRACTIC TABLEProgressive Electrical TherapeuticsK940238TUMBLE FORMS JUNIOR TRISTANDERCamp Intl., Inc.K932233ECONOMY HI-LOW WORK TABLE (MANUAL) MODEL 3405Bailey Mfg. Co.

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.

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