FDA 510(k)

INOX IORCEPS JAR

K-Number: K852302 · 1985-07-02

Decision Date1985-07-02

Product Code

DecisionSubstantially Equivalent

Device Summary

INOX IORCEPS JAR is the device name listed in this FDA 510(k) record. The listed applicant is Broadwest Corp.. It received FDA 510(k) clearance on 1985-07-02 under 510(k) number K852302. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INOX IORCEPS JAR?

INOX IORCEPS JAR is a medical device that received FDA 510(k) clearance on 1985-07-02. The listed applicant is Broadwest Corp.. The 510(k) number is K852302.

When did INOX IORCEPS JAR receive FDA 510(k) clearance?

INOX IORCEPS JAR received FDA 510(k) clearance on 1985-07-02, under 510(k) number K852302.

Who is the listed applicant for INOX IORCEPS JAR?

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

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Other records listing Broadwest Corp. as applicant

K864499PODOSCOPE K864569PODODIGITAL K852301INOX THERMOMETER JAR K852300INOX IV STAND K851307INOX DRY HEAT STERILIZER

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.