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FDA 510(k)

MULTIPLE OUTLET MANIFOLD

K-Number: K850389 · 1985-03-18

ApplicantThe Anspach Effort, Inc.
Decision Date1985-03-18
Product CodeGEY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MULTIPLE OUTLET MANIFOLD is the device name listed in this FDA 510(k) record. The listed applicant is The Anspach Effort, Inc.. It received FDA 510(k) clearance on 1985-03-18 under 510(k) number K850389. The device is classified under product code GEY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIPLE OUTLET MANIFOLD?

MULTIPLE OUTLET MANIFOLD is a medical device that received FDA 510(k) clearance on 1985-03-18. The listed applicant is The Anspach Effort, Inc.. The 510(k) number is K850389.

When did MULTIPLE OUTLET MANIFOLD receive FDA 510(k) clearance?

MULTIPLE OUTLET MANIFOLD received FDA 510(k) clearance on 1985-03-18, under 510(k) number K850389.

Who is the listed applicant for MULTIPLE OUTLET MANIFOLD?

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

What is the FDA product code for MULTIPLE OUTLET MANIFOLD?

The FDA product code for MULTIPLE OUTLET MANIFOLD is GEY.

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Other records listing The Anspach Effort, Inc. as applicant

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Related Devices (Code: GEY)

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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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