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FDA 510(k)

CM-TRISACRYL M DEAE-TRISACRYL M

K-Number: K842028 · 1984-06-07

ApplicantLkb Instruments, Inc.
Decision Date1984-06-07
Product CodeKEA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CM-TRISACRYL M DEAE-TRISACRYL M is the device name listed in this FDA 510(k) record. The listed applicant is Lkb Instruments, Inc.. It received FDA 510(k) clearance on 1984-06-07 under 510(k) number K842028. The device is classified under product code KEA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CM-TRISACRYL M DEAE-TRISACRYL M?

CM-TRISACRYL M DEAE-TRISACRYL M is a medical device that received FDA 510(k) clearance on 1984-06-07. The listed applicant is Lkb Instruments, Inc.. The 510(k) number is K842028.

When did CM-TRISACRYL M DEAE-TRISACRYL M receive FDA 510(k) clearance?

CM-TRISACRYL M DEAE-TRISACRYL M received FDA 510(k) clearance on 1984-06-07, under 510(k) number K842028.

Who is the listed applicant for CM-TRISACRYL M DEAE-TRISACRYL M?

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

What is the FDA product code for CM-TRISACRYL M DEAE-TRISACRYL M?

The FDA product code for CM-TRISACRYL M DEAE-TRISACRYL M is KEA.

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Related Devices (Code: KEA)

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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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