MULTIDEX GEL
K-Number: K952774 · 1995-07-24
Device Summary
Frequently Asked Questions
What is the MULTIDEX GEL?
MULTIDEX GEL is a medical device that received FDA 510(k) clearance on 1995-07-24. The listed applicant is Lange Medical Products, Inc.. The 510(k) number is K952774.
When did MULTIDEX GEL receive FDA 510(k) clearance?
MULTIDEX GEL received FDA 510(k) clearance on 1995-07-24, under 510(k) number K952774.
Who is the listed applicant for MULTIDEX GEL?
The FDA 510(k) record lists Lange Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MULTIDEX GEL?
The FDA product code for MULTIDEX GEL is MGQ.
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 Lange Medical Products, 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: MGQ)
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.