CATALOG #4-2520 CHLORIDOMETER CHLORIDE
K-Number: K791312 · 1979-08-16
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Device Summary
Frequently Asked Questions
What is the CATALOG #4-2520 CHLORIDOMETER CHLORIDE?
CATALOG #4-2520 CHLORIDOMETER CHLORIDE is a medical device that received FDA 510(k) clearance on 1979-08-16. The listed applicant is Buchler Instruments, Inc.. The 510(k) number is K791312.
When did CATALOG #4-2520 CHLORIDOMETER CHLORIDE receive FDA 510(k) clearance?
CATALOG #4-2520 CHLORIDOMETER CHLORIDE received FDA 510(k) clearance on 1979-08-16, under 510(k) number K791312.
Who is the listed applicant for CATALOG #4-2520 CHLORIDOMETER CHLORIDE?
The FDA 510(k) record lists Buchler Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CATALOG #4-2520 CHLORIDOMETER CHLORIDE?
The FDA product code for CATALOG #4-2520 CHLORIDOMETER CHLORIDE is JIT.
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 Buchler Instruments, 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: JIT)
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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