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FDA 510(k)

REUSABLE, DISPOSABLE LAPAROSCOPIC INSTRUMENT AND SURGICAL DEVICE AND ACCESSORIES

K-Number: K072753 · 2008-01-25

ApplicantRg Medical USA
Decision Date2008-01-25
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

REUSABLE, DISPOSABLE LAPAROSCOPIC INSTRUMENT AND SURGICAL DEVICE AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Rg Medical USA. It received FDA 510(k) clearance on 2008-01-25 under 510(k) number K072753. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REUSABLE, DISPOSABLE LAPAROSCOPIC INSTRUMENT AND SURGICAL DEVICE AND ACCESSORIES?

REUSABLE, DISPOSABLE LAPAROSCOPIC INSTRUMENT AND SURGICAL DEVICE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 2008-01-25. The listed applicant is Rg Medical USA. The 510(k) number is K072753.

When did REUSABLE, DISPOSABLE LAPAROSCOPIC INSTRUMENT AND SURGICAL DEVICE AND ACCESSORIES receive FDA 510(k) clearance?

REUSABLE, DISPOSABLE LAPAROSCOPIC INSTRUMENT AND SURGICAL DEVICE AND ACCESSORIES received FDA 510(k) clearance on 2008-01-25, under 510(k) number K072753.

Who is the listed applicant for REUSABLE, DISPOSABLE LAPAROSCOPIC INSTRUMENT AND SURGICAL DEVICE AND ACCESSORIES?

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

What is the FDA product code for REUSABLE, DISPOSABLE LAPAROSCOPIC INSTRUMENT AND SURGICAL DEVICE AND ACCESSORIES?

The FDA product code for REUSABLE, DISPOSABLE LAPAROSCOPIC INSTRUMENT AND SURGICAL DEVICE AND ACCESSORIES is HIF.

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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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