FDA 510(k)

ENDO-TECH LTD., TIPS

K-Number: K961695 · 1996-07-01

Decision Date1996-07-01

Product CodeHFG

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

ENDO-TECH LTD., TIPS is the device name listed in this FDA 510(k) record. The listed applicant is Ratio Design Lab. It received FDA 510(k) clearance on 1996-07-01 under 510(k) number K961695. The device is classified under product code HFG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDO-TECH LTD., TIPS?

ENDO-TECH LTD., TIPS is a medical device that received FDA 510(k) clearance on 1996-07-01. The listed applicant is Ratio Design Lab. The 510(k) number is K961695.

When did ENDO-TECH LTD., TIPS receive FDA 510(k) clearance?

ENDO-TECH LTD., TIPS received FDA 510(k) clearance on 1996-07-01, under 510(k) number K961695.

Who is the listed applicant for ENDO-TECH LTD., TIPS?

The FDA 510(k) record lists Ratio Design Lab as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDO-TECH LTD., TIPS?

The FDA product code for ENDO-TECH LTD., TIPS is HFG.

Related Devices (Code: HFG)

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.

K181124Acessa ProVu SystemAcessa Health, Inc.K121858THE ABLATION SYSTEMHalt Medical, Inc.K101606MICROMED PD-8K INSULATION DEFECT DETECTORMcgan Technology, LLC K991424INSULSCAN INSULATION TESTING SYSTEMMedicor Corp.K921405DAVOL SUCTION/IRRIGATOR W/ INTERCHANGEABLE TIPDavol, Inc.K915406DAVOL ELECTROSUGICAL PROBESDavol, Inc.

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.