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FDA 510(k)

MEDLINE RADIOLOGY-DIAGNOSTIC KITS

K-Number: K962826 · 1996-09-16

ApplicantMedline Industries, Inc.
Decision Date1996-09-16
Product CodeLRO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDLINE RADIOLOGY-DIAGNOSTIC KITS 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 1996-09-16 under 510(k) number K962826. The device is classified under product code LRO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDLINE RADIOLOGY-DIAGNOSTIC KITS?

MEDLINE RADIOLOGY-DIAGNOSTIC KITS is a medical device that received FDA 510(k) clearance on 1996-09-16. The listed applicant is Medline Industries, Inc.. The 510(k) number is K962826.

When did MEDLINE RADIOLOGY-DIAGNOSTIC KITS receive FDA 510(k) clearance?

MEDLINE RADIOLOGY-DIAGNOSTIC KITS received FDA 510(k) clearance on 1996-09-16, under 510(k) number K962826.

Who is the listed applicant for MEDLINE RADIOLOGY-DIAGNOSTIC KITS?

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 RADIOLOGY-DIAGNOSTIC KITS?

The FDA product code for MEDLINE RADIOLOGY-DIAGNOSTIC KITS is LRO.

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Other records listing Medline Industries, Inc. as applicant

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Related Devices (Code: LRO)

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.

K213481Medline General Surgery TrayMedline Industries, Inc.K212258Medline Cardiovascular Procedure KitMedline Industries, Inc.K041080SURGICAL DRAPE KIT - D.I.R.R.A. SRLD.I.R.R.A. S.R.L.K030721QUICK-TAP PARACENTESIS TRAY, KIT & NEEDLEBallard Medical ProductsK023276AMSINO TRACHEOSTOMY CARE TRAYAmsino International, Inc.K980137WORLDWIDE MEDICAL TECHNOLOGIES BONE MARROW BIOPSY PROCEDURE TRAYWorldwide Medical Technologies, LLC

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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