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FDA 510(k)

MEDLINE CATHETERIZATION LABORATORY TRAYS/KITS/PACKS

K-Number: K965112 · 1997-10-10

Decision Date1997-10-10
Product CodeDQO
Advisory CommitteeCV
DecisionUnknown

Device Summary

MEDLINE CATHETERIZATION LABORATORY TRAYS/KITS/PACKS is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 1997-10-10 under 510(k) number K965112. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MEDLINE CATHETERIZATION LABORATORY TRAYS/KITS/PACKS?

MEDLINE CATHETERIZATION LABORATORY TRAYS/KITS/PACKS is a medical device that received FDA 510(k) clearance on 1997-10-10. The listed applicant is Medline Industries, Inc.. The 510(k) number is K965112.

When did MEDLINE CATHETERIZATION LABORATORY TRAYS/KITS/PACKS receive FDA 510(k) clearance?

MEDLINE CATHETERIZATION LABORATORY TRAYS/KITS/PACKS received FDA 510(k) clearance on 1997-10-10, under 510(k) number K965112.

Who is the listed applicant for MEDLINE CATHETERIZATION LABORATORY TRAYS/KITS/PACKS?

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

What is the FDA product code for MEDLINE CATHETERIZATION LABORATORY TRAYS/KITS/PACKS?

The FDA product code for MEDLINE CATHETERIZATION LABORATORY TRAYS/KITS/PACKS is DQO.

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.

Other records listing Medline Industries, 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.

View all 223 devices →

Related Devices (Code: DQO)

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.

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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