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FDA 510(k)

MICRODISCECTOMY CURRETTES

K-Number: K882077 · 1988-06-17

ApplicantKarlin Technology, Inc.
Decision Date1988-06-17
Product CodeLXH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MICRODISCECTOMY CURRETTES is the device name listed in this FDA 510(k) record. The listed applicant is Karlin Technology, Inc.. It received FDA 510(k) clearance on 1988-06-17 under 510(k) number K882077. The device is classified under product code LXH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRODISCECTOMY CURRETTES?

MICRODISCECTOMY CURRETTES is a medical device that received FDA 510(k) clearance on 1988-06-17. The listed applicant is Karlin Technology, Inc.. The 510(k) number is K882077.

When did MICRODISCECTOMY CURRETTES receive FDA 510(k) clearance?

MICRODISCECTOMY CURRETTES received FDA 510(k) clearance on 1988-06-17, under 510(k) number K882077.

Who is the listed applicant for MICRODISCECTOMY CURRETTES?

The FDA 510(k) record lists Karlin Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICRODISCECTOMY CURRETTES?

The FDA product code for MICRODISCECTOMY CURRETTES is LXH.

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Other records listing Karlin Technology, Inc. as applicant

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Related Devices (Code: LXH)

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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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