DYNAMIC PRESSURE MONITOR 2000M AND 2000C
K-Number: K925258 · 1993-03-09
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Device Summary
Frequently Asked Questions
What is the DYNAMIC PRESSURE MONITOR 2000M AND 2000C?
DYNAMIC PRESSURE MONITOR 2000M AND 2000C is a medical device that received FDA 510(k) clearance on 1993-03-09. The listed applicant is Pin Dot Products, Inc.. The 510(k) number is K925258.
When did DYNAMIC PRESSURE MONITOR 2000M AND 2000C receive FDA 510(k) clearance?
DYNAMIC PRESSURE MONITOR 2000M AND 2000C received FDA 510(k) clearance on 1993-03-09, under 510(k) number K925258.
Who is the listed applicant for DYNAMIC PRESSURE MONITOR 2000M AND 2000C?
The FDA 510(k) record lists Pin Dot Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DYNAMIC PRESSURE MONITOR 2000M AND 2000C?
The FDA product code for DYNAMIC PRESSURE MONITOR 2000M AND 2000C is JFC.
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 Pin Dot 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: JFC)
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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