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FDA 510(k)

DEDO SUCTION CANNULA

K-Number: K854005 · 1985-12-06

ApplicantDedo Manufacturer, Inc.
Decision Date1985-12-06
Product CodeGEA
Advisory CommitteeSU
DecisionSubstantially Equivalent for Some Indications

Device Summary

DEDO SUCTION CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Dedo Manufacturer, Inc.. It received FDA 510(k) clearance on 1985-12-06 under 510(k) number K854005. The device is classified under product code GEA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the DEDO SUCTION CANNULA?

DEDO SUCTION CANNULA is a medical device that received FDA 510(k) clearance on 1985-12-06. The listed applicant is Dedo Manufacturer, Inc.. The 510(k) number is K854005.

When did DEDO SUCTION CANNULA receive FDA 510(k) clearance?

DEDO SUCTION CANNULA received FDA 510(k) clearance on 1985-12-06, under 510(k) number K854005.

Who is the listed applicant for DEDO SUCTION CANNULA?

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

What is the FDA product code for DEDO SUCTION CANNULA?

The FDA product code for DEDO SUCTION CANNULA is GEA.

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Related Devices (Code: GEA)

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.

K003965MRI SAFE INSTRUMENTSAesculap, Inc.K982472GENICON TROCARGenicon, LCK954599CONMED TROGARD ELECTRONIC TROCAR SYSTEMConmedcorpK922460ORIGIN SECONDARY CANNULA AND TROCAROrigin Medsystems, Inc.K920110ENDOPATH DISPOSABLE THORACIC TROCAR SLEEVEETHICON, Inc.K911262DISPOSABLE SPECIMEN BAG W/CANNULA AND INTRODUCERETHICON, 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.

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