CARTRIDGE HOLDER, RCM 100
K-Number: K782175 · 1979-02-15
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Device Summary
Frequently Asked Questions
What is the CARTRIDGE HOLDER, RCM 100?
CARTRIDGE HOLDER, RCM 100 is a medical device that received FDA 510(k) clearance on 1979-02-15. The listed applicant is Waters Assoc., Inc.. The 510(k) number is K782175.
When did CARTRIDGE HOLDER, RCM 100 receive FDA 510(k) clearance?
CARTRIDGE HOLDER, RCM 100 received FDA 510(k) clearance on 1979-02-15, under 510(k) number K782175.
Who is the listed applicant for CARTRIDGE HOLDER, RCM 100?
The FDA 510(k) record lists Waters Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CARTRIDGE HOLDER, RCM 100?
The FDA product code for CARTRIDGE HOLDER, RCM 100 is KIE.
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 Waters Assoc., 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: KIE)
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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