IMMUNOPLATE III RADIO IMMUNODIFFUSION
K-Number: K770548 · 1977-04-15
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Device Summary
Frequently Asked Questions
What is the IMMUNOPLATE III RADIO IMMUNODIFFUSION?
IMMUNOPLATE III RADIO IMMUNODIFFUSION is a medical device that received FDA 510(k) clearance on 1977-04-15. The listed applicant is Hyland Therapeutic Div., Travenol Laboratories. The 510(k) number is K770548.
When did IMMUNOPLATE III RADIO IMMUNODIFFUSION receive FDA 510(k) clearance?
IMMUNOPLATE III RADIO IMMUNODIFFUSION received FDA 510(k) clearance on 1977-04-15, under 510(k) number K770548.
Who is the listed applicant for IMMUNOPLATE III RADIO IMMUNODIFFUSION?
The FDA 510(k) record lists Hyland Therapeutic Div., Travenol Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IMMUNOPLATE III RADIO IMMUNODIFFUSION?
The FDA product code for IMMUNOPLATE III RADIO IMMUNODIFFUSION is JZQ.
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 Hyland Therapeutic Div., Travenol Laboratories 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: JZQ)
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.
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