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FDA 510(k)

JOHNSON & JOHNSON DUAL SYRINGE APPLICATOR

K-Number: K902157 · 1990-11-29

ApplicantJohnson & Johnson Medical, Inc.
Decision Date1990-11-29
Product CodeFMF
Advisory CommitteeHO
DecisionUnknown

Device Summary

JOHNSON & JOHNSON DUAL SYRINGE APPLICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Medical, Inc.. It received FDA 510(k) clearance on 1990-11-29 under 510(k) number K902157. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the JOHNSON & JOHNSON DUAL SYRINGE APPLICATOR?

JOHNSON & JOHNSON DUAL SYRINGE APPLICATOR is a medical device that received FDA 510(k) clearance on 1990-11-29. The listed applicant is Johnson & Johnson Medical, Inc.. The 510(k) number is K902157.

When did JOHNSON & JOHNSON DUAL SYRINGE APPLICATOR receive FDA 510(k) clearance?

JOHNSON & JOHNSON DUAL SYRINGE APPLICATOR received FDA 510(k) clearance on 1990-11-29, under 510(k) number K902157.

Who is the listed applicant for JOHNSON & JOHNSON DUAL SYRINGE APPLICATOR?

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

What is the FDA product code for JOHNSON & JOHNSON DUAL SYRINGE APPLICATOR?

The FDA product code for JOHNSON & JOHNSON DUAL SYRINGE APPLICATOR is FMF.

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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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