SPECTRUM 2 REUSABLE FULL FACE MASK, MODEL 1004884 AND 1004876
K-Number: K002465 · 2000-09-08
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Device Summary
Frequently Asked Questions
What is the SPECTRUM 2 REUSABLE FULL FACE MASK, MODEL 1004884 AND 1004876?
SPECTRUM 2 REUSABLE FULL FACE MASK, MODEL 1004884 AND 1004876 is a medical device that received FDA 510(k) clearance on 2000-09-08. The listed applicant is Respironics, Inc.. The 510(k) number is K002465.
When did SPECTRUM 2 REUSABLE FULL FACE MASK, MODEL 1004884 AND 1004876 receive FDA 510(k) clearance?
SPECTRUM 2 REUSABLE FULL FACE MASK, MODEL 1004884 AND 1004876 received FDA 510(k) clearance on 2000-09-08, under 510(k) number K002465.
Who is the listed applicant for SPECTRUM 2 REUSABLE FULL FACE MASK, MODEL 1004884 AND 1004876?
The FDA 510(k) record lists Respironics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SPECTRUM 2 REUSABLE FULL FACE MASK, MODEL 1004884 AND 1004876?
The FDA product code for SPECTRUM 2 REUSABLE FULL FACE MASK, MODEL 1004884 AND 1004876 is BZD.
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 Respironics, 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.
Related Devices (Code: BZD)
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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