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FDA 510(k)

BEBIG PLAQUES RUM101-RUM114

K-Number: K931393 · 1994-03-16

ApplicantBebig, Inc.
Decision Date1994-03-16
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BEBIG PLAQUES RUM101-RUM114 is the device name listed in this FDA 510(k) record. The listed applicant is Bebig, Inc.. It received FDA 510(k) clearance on 1994-03-16 under 510(k) number K931393. The device is classified under product code KXK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEBIG PLAQUES RUM101-RUM114?

BEBIG PLAQUES RUM101-RUM114 is a medical device that received FDA 510(k) clearance on 1994-03-16. The listed applicant is Bebig, Inc.. The 510(k) number is K931393.

When did BEBIG PLAQUES RUM101-RUM114 receive FDA 510(k) clearance?

BEBIG PLAQUES RUM101-RUM114 received FDA 510(k) clearance on 1994-03-16, under 510(k) number K931393.

Who is the listed applicant for BEBIG PLAQUES RUM101-RUM114?

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

What is the FDA product code for BEBIG PLAQUES RUM101-RUM114?

The FDA product code for BEBIG PLAQUES RUM101-RUM114 is KXK.

Related Clinical Trials

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.

Related Devices (Code: KXK)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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