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FDA 510(k)

PAEDISCOPE, MODEL # P010A AND PF011A

K-Number: K014149 · 2002-03-18

ApplicantAesculap, Inc.
Decision Date2002-03-18
Product CodeGWG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

PAEDISCOPE, MODEL # P010A AND PF011A is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap, Inc.. It received FDA 510(k) clearance on 2002-03-18 under 510(k) number K014149. The device is classified under product code GWG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAEDISCOPE, MODEL # P010A AND PF011A?

PAEDISCOPE, MODEL # P010A AND PF011A is a medical device that received FDA 510(k) clearance on 2002-03-18. The listed applicant is Aesculap, Inc.. The 510(k) number is K014149.

When did PAEDISCOPE, MODEL # P010A AND PF011A receive FDA 510(k) clearance?

PAEDISCOPE, MODEL # P010A AND PF011A received FDA 510(k) clearance on 2002-03-18, under 510(k) number K014149.

Who is the listed applicant for PAEDISCOPE, MODEL # P010A AND PF011A?

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

What is the FDA product code for PAEDISCOPE, MODEL # P010A AND PF011A?

The FDA product code for PAEDISCOPE, MODEL # P010A AND PF011A is GWG.

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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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