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FDA 510(k)

FLUSHFLO-MODEL CC1-6

K-Number: K761273 · 1977-01-12

ApplicantBentley Laboratories, Inc.
Decision Date1977-01-12
Product CodeKRA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

FLUSHFLO-MODEL CC1-6 is the device name listed in this FDA 510(k) record. The listed applicant is Bentley Laboratories, Inc.. It received FDA 510(k) clearance on 1977-01-12 under 510(k) number K761273. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLUSHFLO-MODEL CC1-6?

FLUSHFLO-MODEL CC1-6 is a medical device that received FDA 510(k) clearance on 1977-01-12. The listed applicant is Bentley Laboratories, Inc.. The 510(k) number is K761273.

When did FLUSHFLO-MODEL CC1-6 receive FDA 510(k) clearance?

FLUSHFLO-MODEL CC1-6 received FDA 510(k) clearance on 1977-01-12, under 510(k) number K761273.

Who is the listed applicant for FLUSHFLO-MODEL CC1-6?

The FDA 510(k) record lists Bentley Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLUSHFLO-MODEL CC1-6?

The FDA product code for FLUSHFLO-MODEL CC1-6 is KRA.

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Related Devices (Code: KRA)

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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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