FDA 510(k)

SPRING RETRACTOR

K-Number: K880997 · 1988-03-21

ApplicantT. Korossurgical Instruments Corp.

Decision Date1988-03-21

Product CodeGAD

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

SPRING 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 1988-03-21 under 510(k) number K880997. 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 SPRING RETRACTOR?

SPRING RETRACTOR is a medical device that received FDA 510(k) clearance on 1988-03-21. The listed applicant is T. Korossurgical Instruments Corp.. The 510(k) number is K880997.

When did SPRING RETRACTOR receive FDA 510(k) clearance?

SPRING RETRACTOR received FDA 510(k) clearance on 1988-03-21, under 510(k) number K880997.

Who is the listed applicant for SPRING 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 SPRING RETRACTOR?

The FDA product code for SPRING RETRACTOR is GAD.

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Other records listing T. Korossurgical Instruments 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.