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FDA 510(k)

STREAM-SWITCH MANIFOLD

K-Number: K861209 · 1986-06-23

ApplicantIntelligent Medicine, Inc.
Decision Date1986-06-23
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STREAM-SWITCH MANIFOLD is the device name listed in this FDA 510(k) record. The listed applicant is Intelligent Medicine, Inc.. It received FDA 510(k) clearance on 1986-06-23 under 510(k) number K861209. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STREAM-SWITCH MANIFOLD?

STREAM-SWITCH MANIFOLD is a medical device that received FDA 510(k) clearance on 1986-06-23. The listed applicant is Intelligent Medicine, Inc.. The 510(k) number is K861209.

When did STREAM-SWITCH MANIFOLD receive FDA 510(k) clearance?

STREAM-SWITCH MANIFOLD received FDA 510(k) clearance on 1986-06-23, under 510(k) number K861209.

Who is the listed applicant for STREAM-SWITCH MANIFOLD?

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

What is the FDA product code for STREAM-SWITCH MANIFOLD?

The FDA product code for STREAM-SWITCH MANIFOLD is FRN.

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Other records listing Intelligent Medicine, 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.

K861598INTELLIGRAPH(TM) PROGRAMMERK861208INTELLIJECT MEDICATION SYRINGEK861207INTELLIJECT INFUSION PUMP

Related Devices (Code: FRN)

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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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