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FDA 510(k)

INVAC W/VARIOUS MODELS

K-Number: K831116 · 1983-08-12

ApplicantPmt
Decision Date1983-08-12
Product CodeGCX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INVAC W/VARIOUS MODELS is the device name listed in this FDA 510(k) record. The listed applicant is Pmt. It received FDA 510(k) clearance on 1983-08-12 under 510(k) number K831116. The device is classified under product code GCX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INVAC W/VARIOUS MODELS?

INVAC W/VARIOUS MODELS is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is Pmt. The 510(k) number is K831116.

When did INVAC W/VARIOUS MODELS receive FDA 510(k) clearance?

INVAC W/VARIOUS MODELS received FDA 510(k) clearance on 1983-08-12, under 510(k) number K831116.

Who is the listed applicant for INVAC W/VARIOUS MODELS?

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

What is the FDA product code for INVAC W/VARIOUS MODELS?

The FDA product code for INVAC W/VARIOUS MODELS is GCX.

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.

Related Devices (Code: GCX)

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

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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