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)

DISPOSABLE SURGICAL FACE MASK

K-Number: K875172 · 1988-01-22

Decision Date1988-01-22
Product CodeFXX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE SURGICAL FACE MASK is the device name listed in this FDA 510(k) record. The listed applicant is Irema USA , Ltd.. It received FDA 510(k) clearance on 1988-01-22 under 510(k) number K875172. The device is classified under product code FXX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE SURGICAL FACE MASK?

DISPOSABLE SURGICAL FACE MASK is a medical device that received FDA 510(k) clearance on 1988-01-22. The listed applicant is Irema USA , Ltd.. The 510(k) number is K875172.

When did DISPOSABLE SURGICAL FACE MASK receive FDA 510(k) clearance?

DISPOSABLE SURGICAL FACE MASK received FDA 510(k) clearance on 1988-01-22, under 510(k) number K875172.

Who is the listed applicant for DISPOSABLE SURGICAL FACE MASK?

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

What is the FDA product code for DISPOSABLE SURGICAL FACE MASK?

The FDA product code for DISPOSABLE SURGICAL FACE MASK is FXX.

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 Irema USA , Ltd. 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.

Related Devices (Code: FXX)

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.

↑