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FDA 510(k)

READYCATH CATHETER

K-Number: K973120 · 1998-02-25

ApplicantMedical Technologies of Georgia
Decision Date1998-02-25
Product CodeGBM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

READYCATH CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Technologies of Georgia. It received FDA 510(k) clearance on 1998-02-25 under 510(k) number K973120. The device is classified under product code GBM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the READYCATH CATHETER?

READYCATH CATHETER is a medical device that received FDA 510(k) clearance on 1998-02-25. The listed applicant is Medical Technologies of Georgia. The 510(k) number is K973120.

When did READYCATH CATHETER receive FDA 510(k) clearance?

READYCATH CATHETER received FDA 510(k) clearance on 1998-02-25, under 510(k) number K973120.

Who is the listed applicant for READYCATH CATHETER?

The FDA 510(k) record lists Medical Technologies of Georgia as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for READYCATH CATHETER?

The FDA product code for READYCATH CATHETER is GBM.

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Other records listing Medical Technologies of Georgia 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.

K952392MLI SETK911129MMG BILE BAGK873136MMG CATH-N-PLACEK871949MMG DELEE SUCTION CATHETER W/MUCOUS TRAPK854821MMG EXTERNAL FEMALE CATHETERSK854660THE MMG ENTERAL FEEDING ADMINISTRATION SET

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Related Devices (Code: GBM)

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.

K241734Wellead® Hydrophilic Intermittent Catheter Ready to Use; Wellead® Hydrophilic Intermittent Catheter CompactWell Lead Medical Co., Ltd.K213283GentleCath Air for Men Hydrophilic Intermittent Urinary CatheterConvatec LimitedK211436Intermittent Catheter (Not Finalized)Hollister IncorporatedK200820SpeediCath Compact SetColoplastK192904SpeediCath Compact SetColoplastK200142SpeediCath SoftColoplast

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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