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FDA 510(k)

MILL-ROSE PERCUTANEOUS PROCEDURAL KIT

K-Number: K935858 · 1994-02-22

ApplicantMill-Rose Laboratory
Decision Date1994-02-22
Product CodeLRO
Advisory CommitteeSU
DecisionUnknown

Device Summary

MILL-ROSE PERCUTANEOUS PROCEDURAL KIT is the device name listed in this FDA 510(k) record. The listed applicant is Mill-Rose Laboratory. It received FDA 510(k) clearance on 1994-02-22 under 510(k) number K935858. The device is classified under product code LRO. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MILL-ROSE PERCUTANEOUS PROCEDURAL KIT?

MILL-ROSE PERCUTANEOUS PROCEDURAL KIT is a medical device that received FDA 510(k) clearance on 1994-02-22. The listed applicant is Mill-Rose Laboratory. The 510(k) number is K935858.

When did MILL-ROSE PERCUTANEOUS PROCEDURAL KIT receive FDA 510(k) clearance?

MILL-ROSE PERCUTANEOUS PROCEDURAL KIT received FDA 510(k) clearance on 1994-02-22, under 510(k) number K935858.

Who is the listed applicant for MILL-ROSE PERCUTANEOUS PROCEDURAL KIT?

The FDA 510(k) record lists Mill-Rose Laboratory as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MILL-ROSE PERCUTANEOUS PROCEDURAL KIT?

The FDA product code for MILL-ROSE PERCUTANEOUS PROCEDURAL KIT is LRO.

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Other records listing Mill-Rose Laboratory 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.

K983122MILL-ROSE LABORATORIES TRANSBRONCHIAL NEEDLE ASPIRATION (TBNA) COMBINATION CYTOLOGY/HISTOLOGY PROCEDURAL KITK983124MILL-ROSE LABORATORIES TRANSBRONCHIAL NEEDLE ASPIRATION (TBNA) CYTOLOGY PROCEDURAL KITK971275MILL-ROSE DISPOSABLE POLYPECTOMY SNAREK962736MILL-ROSE LARYNGOSCOPIC INJECTION NEEDLEK960880MILL-ROSE BLIND MICROBIOLOGY BRUSHK954519WANG TRANSENDOSCOPIC ASPIRATION NEEDLE

View all 46 devices →

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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