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FDA 510(k)

HYPRONOSTICON TM

K-Number: K770603 · 1977-09-02

ApplicantOrganon, Inc.
Decision Date1977-09-02
Product CodeJMM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

HYPRONOSTICON TM is the device name listed in this FDA 510(k) record. The listed applicant is Organon, Inc.. It received FDA 510(k) clearance on 1977-09-02 under 510(k) number K770603. The device is classified under product code JMM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYPRONOSTICON TM?

HYPRONOSTICON TM is a medical device that received FDA 510(k) clearance on 1977-09-02. The listed applicant is Organon, Inc.. The 510(k) number is K770603.

When did HYPRONOSTICON TM receive FDA 510(k) clearance?

HYPRONOSTICON TM received FDA 510(k) clearance on 1977-09-02, under 510(k) number K770603.

Who is the listed applicant for HYPRONOSTICON TM?

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

What is the FDA product code for HYPRONOSTICON TM?

The FDA product code for HYPRONOSTICON TM is JMM.

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Other records listing Organon, Inc. as applicant

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Related Devices (Code: JMM)

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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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