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FDA 510(k)

EUTRA GEL FOR WOUND DRESSING

K-Number: K932291 · 1994-07-18

ApplicantSwiss American Products, Inc.
Decision Date1994-07-18
Product CodeMGQ
DecisionSubstantially Equivalent for Some Indications

Device Summary

EUTRA GEL FOR WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Swiss American Products, Inc.. It received FDA 510(k) clearance on 1994-07-18 under 510(k) number K932291. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the EUTRA GEL FOR WOUND DRESSING?

EUTRA GEL FOR WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1994-07-18. The listed applicant is Swiss American Products, Inc.. The 510(k) number is K932291.

When did EUTRA GEL FOR WOUND DRESSING receive FDA 510(k) clearance?

EUTRA GEL FOR WOUND DRESSING received FDA 510(k) clearance on 1994-07-18, under 510(k) number K932291.

Who is the listed applicant for EUTRA GEL FOR WOUND DRESSING?

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

What is the FDA product code for EUTRA GEL FOR WOUND DRESSING?

The FDA product code for EUTRA GEL FOR WOUND DRESSING is MGQ.

Related Clinical Trials

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Other records listing Swiss American Products, Inc. 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.

K103713ELTA WOUND CLEANSERK073610ELTA ADVANCED WOUND WASHK071703ELTA SILVER ANTIMICROBIAL WOUND GEL DRESSING, WOUND AND BURN, HYDROGEL W/DRUG AND/OR BIOLOGIC

Related Devices (Code: MGQ)

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.

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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.

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