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FDA 510(k)

MEDIPALM-20

K-Number: K031202 · 2003-05-01

ApplicantBraebon Medical Corp.
Decision Date2003-05-01
Product CodeOLV
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDIPALM-20 is the device name listed in this FDA 510(k) record. The listed applicant is Braebon Medical Corp.. It received FDA 510(k) clearance on 2003-05-01 under 510(k) number K031202. The device is classified under product code OLV. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIPALM-20?

MEDIPALM-20 is a medical device that received FDA 510(k) clearance on 2003-05-01. The listed applicant is Braebon Medical Corp.. The 510(k) number is K031202.

When did MEDIPALM-20 receive FDA 510(k) clearance?

MEDIPALM-20 received FDA 510(k) clearance on 2003-05-01, under 510(k) number K031202.

Who is the listed applicant for MEDIPALM-20?

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

What is the FDA product code for MEDIPALM-20?

The FDA product code for MEDIPALM-20 is OLV.

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Other records listing Braebon Medical Corp. as applicant

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Related Devices (Code: OLV)

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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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