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FDA 510(k)

(I) LV AND (II) HV SERIES CANNULA

K-Number: K871043 · 1987-04-23

ApplicantCelebration Medical Products, Inc.
Decision Date1987-04-23
Product CodeGEA
Advisory CommitteeSU
DecisionSubstantially Equivalent for Some Indications

Device Summary

(I) LV AND (II) HV SERIES CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Celebration Medical Products, Inc.. It received FDA 510(k) clearance on 1987-04-23 under 510(k) number K871043. 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 (I) LV AND (II) HV SERIES CANNULA?

(I) LV AND (II) HV SERIES CANNULA is a medical device that received FDA 510(k) clearance on 1987-04-23. The listed applicant is Celebration Medical Products, Inc.. The 510(k) number is K871043.

When did (I) LV AND (II) HV SERIES CANNULA receive FDA 510(k) clearance?

(I) LV AND (II) HV SERIES CANNULA received FDA 510(k) clearance on 1987-04-23, under 510(k) number K871043.

Who is the listed applicant for (I) LV AND (II) HV SERIES CANNULA?

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

What is the FDA product code for (I) LV AND (II) HV SERIES CANNULA?

The FDA product code for (I) LV AND (II) HV SERIES 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

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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