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FDA 510(k)

ELECTRIC VACUM PUMP

K-Number: K941096 · 1995-01-05

Decision Date1995-01-05
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECTRIC VACUM PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Impact Instrumentation, Inc.. It received FDA 510(k) clearance on 1995-01-05 under 510(k) number K941096. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRIC VACUM PUMP?

ELECTRIC VACUM PUMP is a medical device that received FDA 510(k) clearance on 1995-01-05. The listed applicant is Impact Instrumentation, Inc.. The 510(k) number is K941096.

When did ELECTRIC VACUM PUMP receive FDA 510(k) clearance?

ELECTRIC VACUM PUMP received FDA 510(k) clearance on 1995-01-05, under 510(k) number K941096.

Who is the listed applicant for ELECTRIC VACUM PUMP?

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

What is the FDA product code for ELECTRIC VACUM PUMP?

The FDA product code for ELECTRIC VACUM PUMP is BTA.

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 Impact Instrumentation, 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 26 devices →

Related Devices (Code: BTA)

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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