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FDA 510(k)

URESIL LAPAROSCOPIC RETRACTOR

K-Number: K921417 · 1993-10-08

ApplicantUresil Corp.
Decision Date1993-10-08
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

URESIL LAPAROSCOPIC RETRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is Uresil Corp.. It received FDA 510(k) clearance on 1993-10-08 under 510(k) number K921417. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URESIL LAPAROSCOPIC RETRACTOR?

URESIL LAPAROSCOPIC RETRACTOR is a medical device that received FDA 510(k) clearance on 1993-10-08. The listed applicant is Uresil Corp.. The 510(k) number is K921417.

When did URESIL LAPAROSCOPIC RETRACTOR receive FDA 510(k) clearance?

URESIL LAPAROSCOPIC RETRACTOR received FDA 510(k) clearance on 1993-10-08, under 510(k) number K921417.

Who is the listed applicant for URESIL LAPAROSCOPIC RETRACTOR?

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

What is the FDA product code for URESIL LAPAROSCOPIC RETRACTOR?

The FDA product code for URESIL LAPAROSCOPIC RETRACTOR is HET.

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Other records listing Uresil Corp. as applicant

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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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