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FDA 510(k)

UROLOGIC TUBE HOLDER

K-Number: K810787 · 1981-03-31

ApplicantThe Urology Group
Decision Date1981-03-31
Product CodeOCV
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

UROLOGIC TUBE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is The Urology Group. It received FDA 510(k) clearance on 1981-03-31 under 510(k) number K810787. The device is classified under product code OCV. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UROLOGIC TUBE HOLDER?

UROLOGIC TUBE HOLDER is a medical device that received FDA 510(k) clearance on 1981-03-31. The listed applicant is The Urology Group. The 510(k) number is K810787.

When did UROLOGIC TUBE HOLDER receive FDA 510(k) clearance?

UROLOGIC TUBE HOLDER received FDA 510(k) clearance on 1981-03-31, under 510(k) number K810787.

Who is the listed applicant for UROLOGIC TUBE HOLDER?

The FDA 510(k) record lists The Urology Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UROLOGIC TUBE HOLDER?

The FDA product code for UROLOGIC TUBE HOLDER is OCV.

Related Clinical Trials

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.

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Other records listing The Urology Group 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.

K831703COVERUPSK831489SURGICAL TUBE HOLDERK810739SUCTION WOUND DRAINAGE DEVICEK810788SURGICAL TUBE HOLDERK801629COVER-ALL MALE INCONTINENCE DEVICE

Related Devices (Code: OCV)

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.

K240506KARL STORZ HoldersKarl Storz Endoscopy America, Inc.K232405ENDOFIX EXOAktormed GmbHK190576WalterLorenz Surgical Assist Arm Scope HolderBiomet MicrofixationK102179ENVIEW (TM)Carefusion 2200K093616V. MUELLER CAMERA CONTROLLER WITH STORAGE CARTCarefusion 2200K992006NEUROVIEW INSTRUMENT HOLDER, MODEL 300-33Integra Neurocare, LLC

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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