SYNERMED LDHH-L REAGENT KIT
K-Number: K921025 · 1992-03-23
Advertisement
Device Summary
Frequently Asked Questions
What is the SYNERMED LDHH-L REAGENT KIT?
SYNERMED LDHH-L REAGENT KIT is a medical device that received FDA 510(k) clearance on 1992-03-23. The listed applicant is Synermed, Inc.. The 510(k) number is K921025.
When did SYNERMED LDHH-L REAGENT KIT receive FDA 510(k) clearance?
SYNERMED LDHH-L REAGENT KIT received FDA 510(k) clearance on 1992-03-23, under 510(k) number K921025.
Who is the listed applicant for SYNERMED LDHH-L REAGENT KIT?
The FDA 510(k) record lists Synermed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYNERMED LDHH-L REAGENT KIT?
The FDA product code for SYNERMED LDHH-L REAGENT KIT is CFJ.
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 Synermed, 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: CFJ)
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