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FDA 510(k)

IMC SALINE WET DRESSING

K-Number: K933774 · 1993-11-08

Decision Date1993-11-08
Product CodeFRO
DecisionSubstantially Equivalent for Some Indications

Device Summary

IMC SALINE WET DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Inman Medical Corp.. It received FDA 510(k) clearance on 1993-11-08 under 510(k) number K933774. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the IMC SALINE WET DRESSING?

IMC SALINE WET DRESSING is a medical device that received FDA 510(k) clearance on 1993-11-08. The listed applicant is Inman Medical Corp.. The 510(k) number is K933774.

When did IMC SALINE WET DRESSING receive FDA 510(k) clearance?

IMC SALINE WET DRESSING received FDA 510(k) clearance on 1993-11-08, under 510(k) number K933774.

Who is the listed applicant for IMC SALINE WET DRESSING?

The FDA 510(k) record lists Inman Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMC SALINE WET DRESSING?

The FDA product code for IMC SALINE WET DRESSING is FRO. This falls under the Anesthesiology category.

Related Clinical Trials

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.

Other records listing Inman Medical Corp. 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.

View all 14 devices →

Related Devices (Code: FRO)

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.

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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