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FDA 510(k)

REDDICK TROCAR AND CANNULA

K-Number: K911601 · 1991-05-21

ApplicantIdeal Medical, Inc.
Decision Date1991-05-21
Product CodeFSM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

REDDICK TROCAR AND CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Ideal Medical, Inc.. It received FDA 510(k) clearance on 1991-05-21 under 510(k) number K911601. The device is classified under product code FSM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REDDICK TROCAR AND CANNULA?

REDDICK TROCAR AND CANNULA is a medical device that received FDA 510(k) clearance on 1991-05-21. The listed applicant is Ideal Medical, Inc.. The 510(k) number is K911601.

When did REDDICK TROCAR AND CANNULA receive FDA 510(k) clearance?

REDDICK TROCAR AND CANNULA received FDA 510(k) clearance on 1991-05-21, under 510(k) number K911601.

Who is the listed applicant for REDDICK TROCAR AND CANNULA?

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

What is the FDA product code for REDDICK TROCAR AND CANNULA?

The FDA product code for REDDICK TROCAR AND CANNULA is FSM.

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Other records listing Ideal Medical, 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.

K944067PEANUT WAND, MODIFICATIONK931115HATCHER STONE-EMBOLIS EXTRACTORK926335IDEAS PEANUT WANDK922161GRICE SOFT TISSUE BIOPSY KITK921922GRICE LAPAROSCOPIC SUTURING NEEDLEK915175REDDICK RETRACTOR

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Related Devices (Code: FSM)

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.

K971217INSTRUMENT TRAY LINERGeneral Hospital Supply Corp.K962328SINGLE USE INSTRUMENT TRAYMedcare Medical Group, Inc.K944025SURGICAL INSTRUMENT TRAYRiley Medical, Inc.K912106ARTHROSCOPY TRAYMedical Device Inspection Co., Inc.K912053OPEN HEART TRAYMedical Device Inspection Co., Inc.K912052HEART CATH TRAYMedical Device Inspection Co., 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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