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FDA 510(k)

UNIVERSAL I.V. HOLDER

K-Number: K821317 · 1982-05-28

ApplicantGeorgetown Medical Co.
Decision Date1982-05-28
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL I.V. HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Georgetown Medical Co.. It received FDA 510(k) clearance on 1982-05-28 under 510(k) number K821317. The device is classified under product code KMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIVERSAL I.V. HOLDER?

UNIVERSAL I.V. HOLDER is a medical device that received FDA 510(k) clearance on 1982-05-28. The listed applicant is Georgetown Medical Co.. The 510(k) number is K821317.

When did UNIVERSAL I.V. HOLDER receive FDA 510(k) clearance?

UNIVERSAL I.V. HOLDER received FDA 510(k) clearance on 1982-05-28, under 510(k) number K821317.

Who is the listed applicant for UNIVERSAL I.V. HOLDER?

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

What is the FDA product code for UNIVERSAL I.V. HOLDER?

The FDA product code for UNIVERSAL I.V. HOLDER is KMK.

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Related Devices (Code: KMK)

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.

K180994SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8FInterrad Medical, Inc.K981860A P HARNESSParaworks Enterprise, Ltd.K963365MULTI-PURPOSE MEDICAL TUBE HOLDERByrd Medical Devices, Inc.K941098SECURE-SITEOp-Co Medical Products , Ltd.K943147STATLOCK CVVenetec, Inc.K943047IV START KITSSterile Concepts, 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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