FDA 510(k)

BARRIER NEURO SHEET

K-Number: K760937 · 1976-12-21

Decision Date1976-12-21

Product CodeKKX

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

BARRIER NEURO SHEET is the device name listed in this FDA 510(k) record. The listed applicant is Surgikos, Inc.. It received FDA 510(k) clearance on 1976-12-21 under 510(k) number K760937. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARRIER NEURO SHEET?

BARRIER NEURO SHEET is a medical device that received FDA 510(k) clearance on 1976-12-21. The listed applicant is Surgikos, Inc.. The 510(k) number is K760937.

When did BARRIER NEURO SHEET receive FDA 510(k) clearance?

BARRIER NEURO SHEET received FDA 510(k) clearance on 1976-12-21, under 510(k) number K760937.

Who is the listed applicant for BARRIER NEURO SHEET?

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

What is the FDA product code for BARRIER NEURO SHEET?

The FDA product code for BARRIER NEURO SHEET is KKX.

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Other records listing Surgikos, Inc. 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.