WAVICIDE MONITOR STRIPS
K-Number: K932047 · 1994-06-02
Advertisement
Device Summary
Frequently Asked Questions
What is the WAVICIDE MONITOR STRIPS?
WAVICIDE MONITOR STRIPS is a medical device that received FDA 510(k) clearance on 1994-06-02. The listed applicant is Serim Research Corp.. The 510(k) number is K932047.
When did WAVICIDE MONITOR STRIPS receive FDA 510(k) clearance?
WAVICIDE MONITOR STRIPS received FDA 510(k) clearance on 1994-06-02, under 510(k) number K932047.
Who is the listed applicant for WAVICIDE MONITOR STRIPS?
The FDA 510(k) record lists Serim Research Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WAVICIDE MONITOR STRIPS?
The FDA product code for WAVICIDE MONITOR STRIPS is MED.
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 Serim Research 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: MED)
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.
Advertisement