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FDA 510(k)

MEDI - PUMP

K-Number: K950867 · 1995-04-19

Decision Date1995-04-19
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MEDI - PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Thomas Industries. It received FDA 510(k) clearance on 1995-04-19 under 510(k) number K950867. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDI - PUMP?

MEDI - PUMP is a medical device that received FDA 510(k) clearance on 1995-04-19. The listed applicant is Thomas Industries. The 510(k) number is K950867.

When did MEDI - PUMP receive FDA 510(k) clearance?

MEDI - PUMP received FDA 510(k) clearance on 1995-04-19, under 510(k) number K950867.

Who is the listed applicant for MEDI - PUMP?

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

What is the FDA product code for MEDI - PUMP?

The FDA product code for MEDI - PUMP is CAF.

Other records listing Thomas Industries 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 9 devices →

Related Devices (Code: CAF)

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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