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FDA 510(k)

INTELLIJECT MEDICATION SYRINGE

K-Number: K861208 · 1986-06-30

ApplicantIntelligent Medicine, Inc.
Decision Date1986-06-30
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INTELLIJECT MEDICATION SYRINGE 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 1986-06-30 under 510(k) number K861208. 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 INTELLIJECT MEDICATION SYRINGE?

INTELLIJECT MEDICATION SYRINGE is a medical device that received FDA 510(k) clearance on 1986-06-30. The listed applicant is Intelligent Medicine, Inc.. The 510(k) number is K861208.

When did INTELLIJECT MEDICATION SYRINGE receive FDA 510(k) clearance?

INTELLIJECT MEDICATION SYRINGE received FDA 510(k) clearance on 1986-06-30, under 510(k) number K861208.

Who is the listed applicant for INTELLIJECT MEDICATION SYRINGE?

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 INTELLIJECT MEDICATION SYRINGE?

The FDA product code for INTELLIJECT MEDICATION SYRINGE is FRN.

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 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) PROGRAMMERK861207INTELLIJECT INFUSION PUMPK861209STREAM-SWITCH MANIFOLD

Related Devices (Code: FRN)

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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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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