MONO-POLY RESOLVING MEDIUM
K-Number: K812947 · 1982-03-11
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Device Summary
Frequently Asked Questions
What is the MONO-POLY RESOLVING MEDIUM?
MONO-POLY RESOLVING MEDIUM is a medical device that received FDA 510(k) clearance on 1982-03-11. The listed applicant is Flow Laboratories, Inc.. The 510(k) number is K812947.
When did MONO-POLY RESOLVING MEDIUM receive FDA 510(k) clearance?
MONO-POLY RESOLVING MEDIUM received FDA 510(k) clearance on 1982-03-11, under 510(k) number K812947.
Who is the listed applicant for MONO-POLY RESOLVING MEDIUM?
The FDA 510(k) record lists Flow Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MONO-POLY RESOLVING MEDIUM?
The FDA product code for MONO-POLY RESOLVING MEDIUM is JCF.
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 Flow 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: JCF)
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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