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FDA 510(k)

P.F.C. APICAL PLUG

K-Number: K944769 · 1994-12-08

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1994-12-08
Product CodeJDL
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

P.F.C. APICAL PLUG is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1994-12-08 under 510(k) number K944769. The device is classified under product code JDL. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the P.F.C. APICAL PLUG?

P.F.C. APICAL PLUG is a medical device that received FDA 510(k) clearance on 1994-12-08. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K944769.

When did P.F.C. APICAL PLUG receive FDA 510(k) clearance?

P.F.C. APICAL PLUG received FDA 510(k) clearance on 1994-12-08, under 510(k) number K944769.

Who is the listed applicant for P.F.C. APICAL PLUG?

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

What is the FDA product code for P.F.C. APICAL PLUG?

The FDA product code for P.F.C. APICAL PLUG is JDL.

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Other records listing Johnson & Johnson Professionals, Inc. as applicant

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Related Devices (Code: JDL)

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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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