SERALYZER HEMOGLOBIN TEST MODULE
K-Number: K822045 · 1982-07-30
Advertisement
Device Summary
Frequently Asked Questions
What is the SERALYZER HEMOGLOBIN TEST MODULE?
SERALYZER HEMOGLOBIN TEST MODULE is a medical device that received FDA 510(k) clearance on 1982-07-30. The listed applicant is Miles Laboratories, Inc.. The 510(k) number is K822045.
When did SERALYZER HEMOGLOBIN TEST MODULE receive FDA 510(k) clearance?
SERALYZER HEMOGLOBIN TEST MODULE received FDA 510(k) clearance on 1982-07-30, under 510(k) number K822045.
Who is the listed applicant for SERALYZER HEMOGLOBIN TEST MODULE?
The FDA 510(k) record lists Miles Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SERALYZER HEMOGLOBIN TEST MODULE?
The FDA product code for SERALYZER HEMOGLOBIN TEST MODULE is KHG.
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 Miles Laboratories, 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: KHG)
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