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FDA 510(k)

PEDABAROGRAPH

K-Number: K861260 · 1986-05-02

ApplicantBiokinetics, Inc.
Decision Date1986-05-02
Product CodeJFC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PEDABAROGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Biokinetics, Inc.. It received FDA 510(k) clearance on 1986-05-02 under 510(k) number K861260. The device is classified under product code JFC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEDABAROGRAPH?

PEDABAROGRAPH is a medical device that received FDA 510(k) clearance on 1986-05-02. The listed applicant is Biokinetics, Inc.. The 510(k) number is K861260.

When did PEDABAROGRAPH receive FDA 510(k) clearance?

PEDABAROGRAPH received FDA 510(k) clearance on 1986-05-02, under 510(k) number K861260.

Who is the listed applicant for PEDABAROGRAPH?

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

What is the FDA product code for PEDABAROGRAPH?

The FDA product code for PEDABAROGRAPH is JFC.

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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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