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FDA 510(k)

HU-FRIEDY IMS CASSETTE SYSTEM

K-Number: K844002 · 1984-11-08

ApplicantHu-Friedy Mfg. Co., Inc.
Decision Date1984-11-08
Product CodeFSM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HU-FRIEDY IMS CASSETTE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Hu-Friedy Mfg. Co., Inc.. It received FDA 510(k) clearance on 1984-11-08 under 510(k) number K844002. 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 HU-FRIEDY IMS CASSETTE SYSTEM?

HU-FRIEDY IMS CASSETTE SYSTEM is a medical device that received FDA 510(k) clearance on 1984-11-08. The listed applicant is Hu-Friedy Mfg. Co., Inc.. The 510(k) number is K844002.

When did HU-FRIEDY IMS CASSETTE SYSTEM receive FDA 510(k) clearance?

HU-FRIEDY IMS CASSETTE SYSTEM received FDA 510(k) clearance on 1984-11-08, under 510(k) number K844002.

Who is the listed applicant for HU-FRIEDY IMS CASSETTE SYSTEM?

The FDA 510(k) record lists Hu-Friedy Mfg. Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HU-FRIEDY IMS CASSETTE SYSTEM?

The FDA product code for HU-FRIEDY IMS CASSETTE SYSTEM is FSM.

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Other records listing Hu-Friedy Mfg. Co., 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.

K100401SWERV MAGNETOSTRICTIVE ULTRASONIC SCALER SYSTEMK073369EI DOWNPAK BARRIER SLEEVESK070975SYMMETRY IQ, MODEL 2000 SERIES, 3000 SERIESK053178SYMMETRY S-SERIES PIEZOELECTRIC SCALING TIPSK012060MODIFICATION TO:HU-FRIEDY BRAND SATIN SWIVEL ULTRASONIC INSERTK953919DENTAL ULTRASONIC SCALER INSERTS

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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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