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FDA 510(k)

ACCU-FLO PRESSURE VALVE

K-Number: K853215 · 1985-09-16

ApplicantCodman & Shurtleff, Inc.
Decision Date1985-09-16
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ACCU-FLO PRESSURE VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1985-09-16 under 510(k) number K853215. The device is classified under product code JXG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCU-FLO PRESSURE VALVE?

ACCU-FLO PRESSURE VALVE is a medical device that received FDA 510(k) clearance on 1985-09-16. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K853215.

When did ACCU-FLO PRESSURE VALVE receive FDA 510(k) clearance?

ACCU-FLO PRESSURE VALVE received FDA 510(k) clearance on 1985-09-16, under 510(k) number K853215.

Who is the listed applicant for ACCU-FLO PRESSURE VALVE?

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

What is the FDA product code for ACCU-FLO PRESSURE VALVE?

The FDA product code for ACCU-FLO PRESSURE VALVE is JXG.

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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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