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FDA 510(k)

PRIMER-P ADHESIVE AGENT

K-Number: K896719 · 1990-02-22

ApplicantParkell
Decision Date1990-02-22
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PRIMER-P ADHESIVE AGENT is the device name listed in this FDA 510(k) record. The listed applicant is Parkell. It received FDA 510(k) clearance on 1990-02-22 under 510(k) number K896719. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRIMER-P ADHESIVE AGENT?

PRIMER-P ADHESIVE AGENT is a medical device that received FDA 510(k) clearance on 1990-02-22. The listed applicant is Parkell. The 510(k) number is K896719.

When did PRIMER-P ADHESIVE AGENT receive FDA 510(k) clearance?

PRIMER-P ADHESIVE AGENT received FDA 510(k) clearance on 1990-02-22, under 510(k) number K896719.

Who is the listed applicant for PRIMER-P ADHESIVE AGENT?

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

What is the FDA product code for PRIMER-P ADHESIVE AGENT?

The FDA product code for PRIMER-P ADHESIVE AGENT is EBI.

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Other records listing Parkell 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.

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