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FDA 510(k)

B. BRAUN IV START KITS

K-Number: K950184 · 1995-03-15

ApplicantB. Braun of America, Inc.
Decision Date1995-03-15
Product CodeLRS
Advisory CommitteeHO
DecisionUnknown

Device Summary

B. BRAUN IV START KITS is the device name listed in this FDA 510(k) record. The listed applicant is B. Braun of America, Inc.. It received FDA 510(k) clearance on 1995-03-15 under 510(k) number K950184. 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 B. BRAUN IV START KITS?

B. BRAUN IV START KITS is a medical device that received FDA 510(k) clearance on 1995-03-15. The listed applicant is B. Braun of America, Inc.. The 510(k) number is K950184.

When did B. BRAUN IV START KITS receive FDA 510(k) clearance?

B. BRAUN IV START KITS received FDA 510(k) clearance on 1995-03-15, under 510(k) number K950184.

Who is the listed applicant for B. BRAUN IV START KITS?

The FDA 510(k) record lists B. Braun of America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for B. BRAUN IV START KITS?

The FDA product code for B. BRAUN IV START KITS is LRS.

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Other records listing B. Braun of America, 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.

K993024CELSITE IMPLANTABLE PORT WITH VALVED CATHETERK983794CHEMO MINI SPIKE PLUSK946170COMFORT-Q SUBCUTANEOUS INJECTION SETSK945850BRAUN DIACAN(R) FISTULA NEEDLESK942988FILTERED EXTENSION SETSK945752CELSITE(TM) BRACHIAL VENOUS PORT

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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.K944041PERSONAL HEARING SYSTEMResound Corp.K943941SAFESTART VASCULAR ACCESS START KITBecton Dickinson Vascular Access, 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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