FDA 510(k)

THE WOOD PUMP 'OLE RED'

K-Number: K855054 · 1986-03-18

Decision Date1986-03-18

Product CodeKZD

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

THE WOOD PUMP 'OLE RED' is the device name listed in this FDA 510(k) record. The listed applicant is T.C. Retigo, Inc.. It received FDA 510(k) clearance on 1986-03-18 under 510(k) number K855054. The device is classified under product code KZD. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE WOOD PUMP 'OLE RED'?

THE WOOD PUMP 'OLE RED' is a medical device that received FDA 510(k) clearance on 1986-03-18. The listed applicant is T.C. Retigo, Inc.. The 510(k) number is K855054.

When did THE WOOD PUMP 'OLE RED' receive FDA 510(k) clearance?

THE WOOD PUMP 'OLE RED' received FDA 510(k) clearance on 1986-03-18, under 510(k) number K855054.

Who is the listed applicant for THE WOOD PUMP 'OLE RED'?

The FDA 510(k) record lists T.C. Retigo, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE WOOD PUMP 'OLE RED'?

The FDA product code for THE WOOD PUMP 'OLE RED' is KZD.

Related Devices (Code: KZD)

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.

K974074INFUSION DYNAMICS POWER INFUSERInfusion Dynamics, Inc.K973843MSI PRESSURE INFUSORSmith Assoc.K953290OLYMPUS AUTOMATIC SURGICAL IRRIGATION PUMPOlympus America, Inc.K951988PRESSURIZERPromedic, Inc.K942933PRESSURE INFUSION CUFFCirculatory Technology, Inc.K930012KAWASUMI LABORATORIES K-CUFFKawasumi Laboratories Co., Ltd.

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.