PURPLE BROTH
K-Number: K851345 · 1985-04-19
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Device Summary
Frequently Asked Questions
What is the PURPLE BROTH?
PURPLE BROTH is a medical device that received FDA 510(k) clearance on 1985-04-19. The listed applicant is Micro Media Laboratories. The 510(k) number is K851345.
When did PURPLE BROTH receive FDA 510(k) clearance?
PURPLE BROTH received FDA 510(k) clearance on 1985-04-19, under 510(k) number K851345.
Who is the listed applicant for PURPLE BROTH?
The FDA 510(k) record lists Micro Media Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PURPLE BROTH?
The FDA product code for PURPLE BROTH is JSH.
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 Micro Media 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: JSH)
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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