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FDA 510(k)

CONTINENT STOMA SYSTEM & ACCESSORIES

K-Number: K844186 · 1985-01-15

ApplicantChesebrough-Pond'S U.S.A. Co.
Decision Date1985-01-15
Product CodeKBG
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

CONTINENT STOMA SYSTEM & ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. It received FDA 510(k) clearance on 1985-01-15 under 510(k) number K844186. The device is classified under product code KBG. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTINENT STOMA SYSTEM & ACCESSORIES?

CONTINENT STOMA SYSTEM & ACCESSORIES is a medical device that received FDA 510(k) clearance on 1985-01-15. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. The 510(k) number is K844186.

When did CONTINENT STOMA SYSTEM & ACCESSORIES receive FDA 510(k) clearance?

CONTINENT STOMA SYSTEM & ACCESSORIES received FDA 510(k) clearance on 1985-01-15, under 510(k) number K844186.

Who is the listed applicant for CONTINENT STOMA SYSTEM & ACCESSORIES?

The FDA 510(k) record lists Chesebrough-Pond'S U.S.A. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONTINENT STOMA SYSTEM & ACCESSORIES?

The FDA product code for CONTINENT STOMA SYSTEM & ACCESSORIES is KBG.

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Other records listing Chesebrough-Pond'S U.S.A. Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K863866RESPIRADYNE II(TM)K862803CHESEBROUGH POND'S HYDROCOLLOID DRESSINGK851382CHESEBROUGH-POND'S SEQUENTIAL WOUND DRESSINGK851383BLISTERFILM TRANSPARENT DRESSINGK851539CHESEBROUGH-PONDS KANGAROO PUMP SET W/EASY-CAP CLOK843567KANGAROO NASOGASTRIC FEEDING TUBE

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Related Devices (Code: KBG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K033591REPROCESSED TROCARSClearmedical, Inc.K013987REPROCESSED DISPOSABLE TROCARSAdven Medical

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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