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FDA 510(k)

VOLUMETRIC PUMP SET 2C9100 FOR NITROGLY

K-Number: K832285 · 1983-12-27

Decision Date1983-12-27
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VOLUMETRIC PUMP SET 2C9100 FOR NITROGLY is the device name listed in this FDA 510(k) record. The listed applicant is Travenol Laboratories, S.A.. It received FDA 510(k) clearance on 1983-12-27 under 510(k) number K832285. 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 VOLUMETRIC PUMP SET 2C9100 FOR NITROGLY?

VOLUMETRIC PUMP SET 2C9100 FOR NITROGLY is a medical device that received FDA 510(k) clearance on 1983-12-27. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K832285.

When did VOLUMETRIC PUMP SET 2C9100 FOR NITROGLY receive FDA 510(k) clearance?

VOLUMETRIC PUMP SET 2C9100 FOR NITROGLY received FDA 510(k) clearance on 1983-12-27, under 510(k) number K832285.

Who is the listed applicant for VOLUMETRIC PUMP SET 2C9100 FOR NITROGLY?

The FDA 510(k) record lists Travenol Laboratories, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VOLUMETRIC PUMP SET 2C9100 FOR NITROGLY?

The FDA product code for VOLUMETRIC PUMP SET 2C9100 FOR NITROGLY 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.

Other records listing Travenol Laboratories, S.A. 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 206 devices →

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.

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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