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FDA 510(k)

LANTOR CUBE STERILIZER TEST PACK

K-Number: K882756 · 1988-10-06

ApplicantLantor Group
Decision Date1988-10-06
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LANTOR CUBE STERILIZER TEST PACK is the device name listed in this FDA 510(k) record. The listed applicant is Lantor Group. It received FDA 510(k) clearance on 1988-10-06 under 510(k) number K882756. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LANTOR CUBE STERILIZER TEST PACK?

LANTOR CUBE STERILIZER TEST PACK is a medical device that received FDA 510(k) clearance on 1988-10-06. The listed applicant is Lantor Group. The 510(k) number is K882756.

When did LANTOR CUBE STERILIZER TEST PACK receive FDA 510(k) clearance?

LANTOR CUBE STERILIZER TEST PACK received FDA 510(k) clearance on 1988-10-06, under 510(k) number K882756.

Who is the listed applicant for LANTOR CUBE STERILIZER TEST PACK?

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

What is the FDA product code for LANTOR CUBE STERILIZER TEST PACK?

The FDA product code for LANTOR CUBE STERILIZER TEST PACK is JOJ.

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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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