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FDA 510(k)

PNEUMATIC ANTERIOR CHAMBER MAINTAINER

K-Number: K830143 · 1983-03-09

ApplicantDiversatronics, Inc.
Decision Date1983-03-09
Product Code
DecisionSubstantially Equivalent

Device Summary

PNEUMATIC ANTERIOR CHAMBER MAINTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Diversatronics, Inc.. It received FDA 510(k) clearance on 1983-03-09 under 510(k) number K830143. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PNEUMATIC ANTERIOR CHAMBER MAINTAINER?

PNEUMATIC ANTERIOR CHAMBER MAINTAINER is a medical device that received FDA 510(k) clearance on 1983-03-09. The listed applicant is Diversatronics, Inc.. The 510(k) number is K830143.

When did PNEUMATIC ANTERIOR CHAMBER MAINTAINER receive FDA 510(k) clearance?

PNEUMATIC ANTERIOR CHAMBER MAINTAINER received FDA 510(k) clearance on 1983-03-09, under 510(k) number K830143.

Who is the listed applicant for PNEUMATIC ANTERIOR CHAMBER MAINTAINER?

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

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 Diversatronics, 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.

K896536PHARMATRONICS NEBULIZERK864015STERILABELS

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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