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FDA 510(k)

CLICK-COUNT U100 INSULIN SYRINGE

K-Number: K833706 · 1984-04-05

Decision Date1984-04-05
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CLICK-COUNT U100 INSULIN SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Orange Medical Instruments, Inc.. It received FDA 510(k) clearance on 1984-04-05 under 510(k) number K833706. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLICK-COUNT U100 INSULIN SYRINGE?

CLICK-COUNT U100 INSULIN SYRINGE is a medical device that received FDA 510(k) clearance on 1984-04-05. The listed applicant is Orange Medical Instruments, Inc.. The 510(k) number is K833706.

When did CLICK-COUNT U100 INSULIN SYRINGE receive FDA 510(k) clearance?

CLICK-COUNT U100 INSULIN SYRINGE received FDA 510(k) clearance on 1984-04-05, under 510(k) number K833706.

Who is the listed applicant for CLICK-COUNT U100 INSULIN SYRINGE?

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

What is the FDA product code for CLICK-COUNT U100 INSULIN SYRINGE?

The FDA product code for CLICK-COUNT U100 INSULIN SYRINGE is FMF.

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.

Other records listing Orange Medical Instruments, 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.

View all 12 devices →

Related Devices (Code: FMF)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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