FDA 510(k)

CIRCUT 1

K-Number: K832147 · 1983-07-26

ApplicantBrimfield Scientific Instruments

Decision Date1983-07-26

Product Code

DecisionSubstantially Equivalent

Device Summary

CIRCUT 1 is the device name listed in this FDA 510(k) record. The listed applicant is Brimfield Scientific Instruments. It received FDA 510(k) clearance on 1983-07-26 under 510(k) number K832147. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CIRCUT 1?

CIRCUT 1 is a medical device that received FDA 510(k) clearance on 1983-07-26. The listed applicant is Brimfield Scientific Instruments. The 510(k) number is K832147.

When did CIRCUT 1 receive FDA 510(k) clearance?

CIRCUT 1 received FDA 510(k) clearance on 1983-07-26, under 510(k) number K832147.

Who is the listed applicant for CIRCUT 1?

The FDA 510(k) record lists Brimfield Scientific Instruments as the applicant. This does not by itself establish the device manufacturer.

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.

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Other records listing Brimfield Scientific Instruments as applicant

K852042BRIMFIELD CANNULATED BLADE HOLDER K843135BRIMFIELD CANNULATED MAGNETIC RETRIEVER K843136BRIMFIELD CANNULATED GRASPING HOOKS K841731BRIMFIELD FIBEROPTIC LIGHT SCOURCE

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.