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FDA 510(k)

DP 100

K-Number: K911192 · 1991-12-11

ApplicantFerguson Medical
Decision Date1991-12-11
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent for Some Indications

Device Summary

DP 100 is the device name listed in this FDA 510(k) record. The listed applicant is Ferguson Medical. It received FDA 510(k) clearance on 1991-12-11 under 510(k) number K911192. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the DP 100?

DP 100 is a medical device that received FDA 510(k) clearance on 1991-12-11. The listed applicant is Ferguson Medical. The 510(k) number is K911192.

When did DP 100 receive FDA 510(k) clearance?

DP 100 received FDA 510(k) clearance on 1991-12-11, under 510(k) number K911192.

Who is the listed applicant for DP 100?

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

What is the FDA product code for DP 100?

The FDA product code for DP 100 is CAF.

Other records listing Ferguson Medical as applicant

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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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