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FDA 510(k)

SAFEBRIS STERILE CIRCUMCISION KIT

K-Number: K902119 · 1990-11-05

ApplicantKedumin Kits, Ltd.
Decision Date1990-11-05
Product CodeFHJ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SAFEBRIS STERILE CIRCUMCISION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Kedumin Kits, Ltd.. It received FDA 510(k) clearance on 1990-11-05 under 510(k) number K902119. The device is classified under product code FHJ. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAFEBRIS STERILE CIRCUMCISION KIT?

SAFEBRIS STERILE CIRCUMCISION KIT is a medical device that received FDA 510(k) clearance on 1990-11-05. The listed applicant is Kedumin Kits, Ltd.. The 510(k) number is K902119.

When did SAFEBRIS STERILE CIRCUMCISION KIT receive FDA 510(k) clearance?

SAFEBRIS STERILE CIRCUMCISION KIT received FDA 510(k) clearance on 1990-11-05, under 510(k) number K902119.

Who is the listed applicant for SAFEBRIS STERILE CIRCUMCISION KIT?

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

What is the FDA product code for SAFEBRIS STERILE CIRCUMCISION KIT?

The FDA product code for SAFEBRIS STERILE CIRCUMCISION KIT is FHJ.

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Related Devices (Code: FHJ)

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.

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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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