FDA 510(k)

MULTIDEX HYDROPHILIC WOUND DRESSING GEL

K-Number: K962917 · 1996-12-16

Decision Date1996-12-16

Product CodeMGQ

DecisionSubstantially Equivalent for Some Indications

Device Summary

MULTIDEX HYDROPHILIC WOUND DRESSING GEL is the device name listed in this FDA 510(k) record. The listed applicant is Lange Medical Products, Inc.. It received FDA 510(k) clearance on 1996-12-16 under 510(k) number K962917. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the MULTIDEX HYDROPHILIC WOUND DRESSING GEL?

MULTIDEX HYDROPHILIC WOUND DRESSING GEL is a medical device that received FDA 510(k) clearance on 1996-12-16. The listed applicant is Lange Medical Products, Inc.. The 510(k) number is K962917.

When did MULTIDEX HYDROPHILIC WOUND DRESSING GEL receive FDA 510(k) clearance?

MULTIDEX HYDROPHILIC WOUND DRESSING GEL received FDA 510(k) clearance on 1996-12-16, under 510(k) number K962917.

Who is the listed applicant for MULTIDEX HYDROPHILIC WOUND DRESSING GEL?

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

What is the FDA product code for MULTIDEX HYDROPHILIC WOUND DRESSING GEL?

The FDA product code for MULTIDEX HYDROPHILIC WOUND DRESSING GEL is MGQ.

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Other records listing Lange Medical Products, Inc. as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.