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FDA 510(k)

DISCOGRAPHY KIT

K-Number: K910503 · 1991-10-07

ApplicantB. Braun of America, Inc.
Decision Date1991-10-07
Product CodeIZG
Advisory CommitteeRA
DecisionUnknown

Device Summary

DISCOGRAPHY KIT 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 1991-10-07 under 510(k) number K910503. The device is classified under product code IZG. It was reviewed by the RA advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the DISCOGRAPHY KIT?

DISCOGRAPHY KIT is a medical device that received FDA 510(k) clearance on 1991-10-07. The listed applicant is B. Braun of America, Inc.. The 510(k) number is K910503.

When did DISCOGRAPHY KIT receive FDA 510(k) clearance?

DISCOGRAPHY KIT received FDA 510(k) clearance on 1991-10-07, under 510(k) number K910503.

Who is the listed applicant for DISCOGRAPHY KIT?

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 DISCOGRAPHY KIT?

The FDA product code for DISCOGRAPHY KIT is IZG.

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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: IZG)

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.

K960082DISCOGRAPHY KITSpinal Specialties, Inc.K960146G.E. STERILE DISPOSABLE RADIOGRAPHIC CONTRAST TRAYGE Medical SystemsK913436PXI PNEUMATIC COMPRESSION PADDLEBrotherston/PxiK920393MU125M MOBILE X-RAY SYSTEMShimadzu Medical SystemsK903808AMSIS RDS, RADIOGRAPHIC DISCOGRAPHY KITAdvanced Med/Surg, Inc.K892659ELECTRODELCAOldelft Corp. of America

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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