PIPETTER-DILUTER (MODEL 273)
K-Number: K761019 · 1976-11-16
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Device Summary
Frequently Asked Questions
What is the PIPETTER-DILUTER (MODEL 273)?
PIPETTER-DILUTER (MODEL 273) is a medical device that received FDA 510(k) clearance on 1976-11-16. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K761019.
When did PIPETTER-DILUTER (MODEL 273) receive FDA 510(k) clearance?
PIPETTER-DILUTER (MODEL 273) received FDA 510(k) clearance on 1976-11-16, under 510(k) number K761019.
Who is the listed applicant for PIPETTER-DILUTER (MODEL 273)?
The FDA 510(k) record lists Beckman Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PIPETTER-DILUTER (MODEL 273)?
The FDA product code for PIPETTER-DILUTER (MODEL 273) is JRW.
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 Beckman 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: JRW)
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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