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FDA 510(k)

PRO-PREP I.V. START/SCRUB-PREP/BLOOD CULTURE KIT

K-Number: K926031 · 1993-06-07

ApplicantBrigam Medical, Inc.
Decision Date1993-06-07
Product CodeLRS
Advisory CommitteeHO
DecisionUnknown

Device Summary

PRO-PREP I.V. START/SCRUB-PREP/BLOOD CULTURE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Brigam Medical, Inc.. It received FDA 510(k) clearance on 1993-06-07 under 510(k) number K926031. The device is classified under product code LRS. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the PRO-PREP I.V. START/SCRUB-PREP/BLOOD CULTURE KIT?

PRO-PREP I.V. START/SCRUB-PREP/BLOOD CULTURE KIT is a medical device that received FDA 510(k) clearance on 1993-06-07. The listed applicant is Brigam Medical, Inc.. The 510(k) number is K926031.

When did PRO-PREP I.V. START/SCRUB-PREP/BLOOD CULTURE KIT receive FDA 510(k) clearance?

PRO-PREP I.V. START/SCRUB-PREP/BLOOD CULTURE KIT received FDA 510(k) clearance on 1993-06-07, under 510(k) number K926031.

Who is the listed applicant for PRO-PREP I.V. START/SCRUB-PREP/BLOOD CULTURE KIT?

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

What is the FDA product code for PRO-PREP I.V. START/SCRUB-PREP/BLOOD CULTURE KIT?

The FDA product code for PRO-PREP I.V. START/SCRUB-PREP/BLOOD CULTURE KIT is LRS.

Related Clinical Trials

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Related Devices (Code: LRS)

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.

K050654AMSINO I.V. START KITAmsino International, Inc.K001879INFUSION IV SETNirvi Intl. USAK963722IV START KITGrand Medical ProductsK951167EMS I.V. START KITEmergency Medical Supply, Inc.K950184B. BRAUN IV START KITSB. Braun of America, Inc.K944041PERSONAL HEARING SYSTEMResound Corp.

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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