PENTAX FACE MASK
K-Number: K933683 · 1995-06-02
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Device Summary
Frequently Asked Questions
What is the PENTAX FACE MASK?
PENTAX FACE MASK is a medical device that received FDA 510(k) clearance on 1995-06-02. The listed applicant is Pentax Precision Instrument Corp.. The 510(k) number is K933683.
When did PENTAX FACE MASK receive FDA 510(k) clearance?
PENTAX FACE MASK received FDA 510(k) clearance on 1995-06-02, under 510(k) number K933683.
Who is the listed applicant for PENTAX FACE MASK?
The FDA 510(k) record lists Pentax Precision Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PENTAX FACE MASK?
The FDA product code for PENTAX 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 Pentax Precision Instrument 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.
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.
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