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FDA 510(k)

RESPIRATOR N95 PARTICULATE RESPIRATOR, MODEL 1730

K-Number: K061375 · 2006-11-17

Decision Date2006-11-17
Product CodeMSH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RESPIRATOR N95 PARTICULATE RESPIRATOR, MODEL 1730 is the device name listed in this FDA 510(k) record. The listed applicant is Louis M. Gerson Co., Inc.. It received FDA 510(k) clearance on 2006-11-17 under 510(k) number K061375. The device is classified under product code MSH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESPIRATOR N95 PARTICULATE RESPIRATOR, MODEL 1730?

RESPIRATOR N95 PARTICULATE RESPIRATOR, MODEL 1730 is a medical device that received FDA 510(k) clearance on 2006-11-17. The listed applicant is Louis M. Gerson Co., Inc.. The 510(k) number is K061375.

When did RESPIRATOR N95 PARTICULATE RESPIRATOR, MODEL 1730 receive FDA 510(k) clearance?

RESPIRATOR N95 PARTICULATE RESPIRATOR, MODEL 1730 received FDA 510(k) clearance on 2006-11-17, under 510(k) number K061375.

Who is the listed applicant for RESPIRATOR N95 PARTICULATE RESPIRATOR, MODEL 1730?

The FDA 510(k) record lists Louis M. Gerson Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RESPIRATOR N95 PARTICULATE RESPIRATOR, MODEL 1730?

The FDA product code for RESPIRATOR N95 PARTICULATE RESPIRATOR, MODEL 1730 is MSH.

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 Louis M. Gerson Co., 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.

View all 8 devices →

Related Devices (Code: MSH)

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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