Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

FERRIS HYDROPHILIC DRESSING

K-Number: K880330 · 1988-03-23

Decision Date1988-03-23
Product CodeFRO
DecisionSubstantially Equivalent for Some Indications

Device Summary

FERRIS HYDROPHILIC DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Ferris Mfg. Corp.. It received FDA 510(k) clearance on 1988-03-23 under 510(k) number K880330. 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 FERRIS HYDROPHILIC DRESSING?

FERRIS HYDROPHILIC DRESSING is a medical device that received FDA 510(k) clearance on 1988-03-23. The listed applicant is Ferris Mfg. Corp.. The 510(k) number is K880330.

When did FERRIS HYDROPHILIC DRESSING receive FDA 510(k) clearance?

FERRIS HYDROPHILIC DRESSING received FDA 510(k) clearance on 1988-03-23, under 510(k) number K880330.

Who is the listed applicant for FERRIS HYDROPHILIC DRESSING?

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

What is the FDA product code for FERRIS HYDROPHILIC DRESSING?

The FDA product code for FERRIS HYDROPHILIC 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 Ferris Mfg. 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 20 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.

↑