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FDA 510(k)

CONFORMA

K-Number: K841559 · 1984-07-17

ApplicantBeiersdorf, Inc.
Decision Date1984-07-17
Product CodeGBI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONFORMA is the device name listed in this FDA 510(k) record. The listed applicant is Beiersdorf, Inc.. It received FDA 510(k) clearance on 1984-07-17 under 510(k) number K841559. The device is classified under product code GBI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONFORMA?

CONFORMA is a medical device that received FDA 510(k) clearance on 1984-07-17. The listed applicant is Beiersdorf, Inc.. The 510(k) number is K841559.

When did CONFORMA receive FDA 510(k) clearance?

CONFORMA received FDA 510(k) clearance on 1984-07-17, under 510(k) number K841559.

Who is the listed applicant for CONFORMA?

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

What is the FDA product code for CONFORMA?

The FDA product code for CONFORMA is GBI.

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Other records listing Beiersdorf, Inc. as applicant

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Related Devices (Code: GBI)

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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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