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FDA 510(k)

MODIFIED LABELING FOR BIOCLUSIVE* TRANS FILM DRESS

K-Number: K901853 · 1991-01-28

ApplicantJohnson & Johnson Medical, Inc.
Decision Date1991-01-28
Product CodeNAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODIFIED LABELING FOR BIOCLUSIVE* TRANS FILM DRESS 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 1991-01-28 under 510(k) number K901853. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED LABELING FOR BIOCLUSIVE* TRANS FILM DRESS?

MODIFIED LABELING FOR BIOCLUSIVE* TRANS FILM DRESS is a medical device that received FDA 510(k) clearance on 1991-01-28. The listed applicant is Johnson & Johnson Medical, Inc.. The 510(k) number is K901853.

When did MODIFIED LABELING FOR BIOCLUSIVE* TRANS FILM DRESS receive FDA 510(k) clearance?

MODIFIED LABELING FOR BIOCLUSIVE* TRANS FILM DRESS received FDA 510(k) clearance on 1991-01-28, under 510(k) number K901853.

Who is the listed applicant for MODIFIED LABELING FOR BIOCLUSIVE* TRANS FILM DRESS?

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 MODIFIED LABELING FOR BIOCLUSIVE* TRANS FILM DRESS?

The FDA product code for MODIFIED LABELING FOR BIOCLUSIVE* TRANS FILM DRESS is NAD.

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

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Related Devices (Code: NAD)

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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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