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FDA 510(k)

JOHNSON & JOHNSON OSTOMY SIZE SELECTOR & BELT

K-Number: K852297 · 1985-06-12

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1985-06-12
Product CodeEXB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

JOHNSON & JOHNSON OSTOMY SIZE SELECTOR & BELT 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 1985-06-12 under 510(k) number K852297. The device is classified under product code EXB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JOHNSON & JOHNSON OSTOMY SIZE SELECTOR & BELT?

JOHNSON & JOHNSON OSTOMY SIZE SELECTOR & BELT is a medical device that received FDA 510(k) clearance on 1985-06-12. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K852297.

When did JOHNSON & JOHNSON OSTOMY SIZE SELECTOR & BELT receive FDA 510(k) clearance?

JOHNSON & JOHNSON OSTOMY SIZE SELECTOR & BELT received FDA 510(k) clearance on 1985-06-12, under 510(k) number K852297.

Who is the listed applicant for JOHNSON & JOHNSON OSTOMY SIZE SELECTOR & BELT?

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 JOHNSON & JOHNSON OSTOMY SIZE SELECTOR & BELT?

The FDA product code for JOHNSON & JOHNSON OSTOMY SIZE SELECTOR & BELT is EXB.

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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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