FDA 510(k)

THOROCOSCOPY SELF-RETAINING RETRACTOR

K-Number: K926585 · 1993-08-06

ApplicantT. Korossurgical Instruments Corp.

Decision Date1993-08-06

Product CodeGAD

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

THOROCOSCOPY SELF-RETAINING RETRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is T. Korossurgical Instruments Corp.. It received FDA 510(k) clearance on 1993-08-06 under 510(k) number K926585. The device is classified under product code GAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THOROCOSCOPY SELF-RETAINING RETRACTOR?

THOROCOSCOPY SELF-RETAINING RETRACTOR is a medical device that received FDA 510(k) clearance on 1993-08-06. The listed applicant is T. Korossurgical Instruments Corp.. The 510(k) number is K926585.

When did THOROCOSCOPY SELF-RETAINING RETRACTOR receive FDA 510(k) clearance?

THOROCOSCOPY SELF-RETAINING RETRACTOR received FDA 510(k) clearance on 1993-08-06, under 510(k) number K926585.

Who is the listed applicant for THOROCOSCOPY SELF-RETAINING RETRACTOR?

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

What is the FDA product code for THOROCOSCOPY SELF-RETAINING RETRACTOR?

The FDA product code for THOROCOSCOPY SELF-RETAINING RETRACTOR is GAD.

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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.