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FDA 510(k)

BEBIG INACTIVE OPHTHALMIC APPLICATORS FOR IODINE 125 SEEDS

K-Number: K945983 · 1995-10-18

ApplicantBebig Trade, Inc.
Decision Date1995-10-18
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BEBIG INACTIVE OPHTHALMIC APPLICATORS FOR IODINE 125 SEEDS is the device name listed in this FDA 510(k) record. The listed applicant is Bebig Trade, Inc.. It received FDA 510(k) clearance on 1995-10-18 under 510(k) number K945983. 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 INACTIVE OPHTHALMIC APPLICATORS FOR IODINE 125 SEEDS?

BEBIG INACTIVE OPHTHALMIC APPLICATORS FOR IODINE 125 SEEDS is a medical device that received FDA 510(k) clearance on 1995-10-18. The listed applicant is Bebig Trade, Inc.. The 510(k) number is K945983.

When did BEBIG INACTIVE OPHTHALMIC APPLICATORS FOR IODINE 125 SEEDS receive FDA 510(k) clearance?

BEBIG INACTIVE OPHTHALMIC APPLICATORS FOR IODINE 125 SEEDS received FDA 510(k) clearance on 1995-10-18, under 510(k) number K945983.

Who is the listed applicant for BEBIG INACTIVE OPHTHALMIC APPLICATORS FOR IODINE 125 SEEDS?

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

What is the FDA product code for BEBIG INACTIVE OPHTHALMIC APPLICATORS FOR IODINE 125 SEEDS?

The FDA product code for BEBIG INACTIVE OPHTHALMIC APPLICATORS FOR IODINE 125 SEEDS is KXK.

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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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