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FDA 510(k)

HYDRAMED BY LECHLER

K-Number: K882953 · 1988-10-12

ApplicantLechler, Inc.
Decision Date1988-10-12
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HYDRAMED BY LECHLER is the device name listed in this FDA 510(k) record. The listed applicant is Lechler, Inc.. It received FDA 510(k) clearance on 1988-10-12 under 510(k) number K882953. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYDRAMED BY LECHLER?

HYDRAMED BY LECHLER is a medical device that received FDA 510(k) clearance on 1988-10-12. The listed applicant is Lechler, Inc.. The 510(k) number is K882953.

When did HYDRAMED BY LECHLER receive FDA 510(k) clearance?

HYDRAMED BY LECHLER received FDA 510(k) clearance on 1988-10-12, under 510(k) number K882953.

Who is the listed applicant for HYDRAMED BY LECHLER?

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

What is the FDA product code for HYDRAMED BY LECHLER?

The FDA product code for HYDRAMED BY LECHLER is CAF.

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Official Source

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