PROGUARD, RR-1, RR-2
K-Number: K982832 · 1998-12-23
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Device Summary
Frequently Asked Questions
What is the PROGUARD, RR-1, RR-2?
PROGUARD, RR-1, RR-2 is a medical device that received FDA 510(k) clearance on 1998-12-23. The listed applicant is Emerson & Co. Srl. The 510(k) number is K982832.
When did PROGUARD, RR-1, RR-2 receive FDA 510(k) clearance?
PROGUARD, RR-1, RR-2 received FDA 510(k) clearance on 1998-12-23, under 510(k) number K982832.
Who is the listed applicant for PROGUARD, RR-1, RR-2?
The FDA 510(k) record lists Emerson & Co. Srl as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROGUARD, RR-1, RR-2?
The FDA product code for PROGUARD, RR-1, RR-2 is LZC.
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 Emerson & Co. Srl 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: LZC)
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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