MODELS 4201, 4231 & 4235 EXTENSION CABLES
K-Number: K902679 · 1990-07-19
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Device Summary
Frequently Asked Questions
What is the MODELS 4201, 4231 & 4235 EXTENSION CABLES?
MODELS 4201, 4231 & 4235 EXTENSION CABLES is a medical device that received FDA 510(k) clearance on 1990-07-19. The listed applicant is Pace Medical. The 510(k) number is K902679.
When did MODELS 4201, 4231 & 4235 EXTENSION CABLES receive FDA 510(k) clearance?
MODELS 4201, 4231 & 4235 EXTENSION CABLES received FDA 510(k) clearance on 1990-07-19, under 510(k) number K902679.
Who is the listed applicant for MODELS 4201, 4231 & 4235 EXTENSION CABLES?
The FDA 510(k) record lists Pace Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODELS 4201, 4231 & 4235 EXTENSION CABLES?
The FDA product code for MODELS 4201, 4231 & 4235 EXTENSION CABLES is DTE.
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 Pace Medical 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: DTE)
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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