MICROFLUOR B REMOVAWELL STRIPS
K-Number: K822962 · 1982-11-16
Advertisement
Device Summary
Frequently Asked Questions
What is the MICROFLUOR B REMOVAWELL STRIPS?
MICROFLUOR B REMOVAWELL STRIPS is a medical device that received FDA 510(k) clearance on 1982-11-16. The listed applicant is Dynatech Corp.. The 510(k) number is K822962.
When did MICROFLUOR B REMOVAWELL STRIPS receive FDA 510(k) clearance?
MICROFLUOR B REMOVAWELL STRIPS received FDA 510(k) clearance on 1982-11-16, under 510(k) number K822962.
Who is the listed applicant for MICROFLUOR B REMOVAWELL STRIPS?
The FDA 510(k) record lists Dynatech Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICROFLUOR B REMOVAWELL STRIPS?
The FDA product code for MICROFLUOR B REMOVAWELL STRIPS is LIB.
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 Dynatech 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: LIB)
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