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FDA 510(k)

RM BOND, MODEL J032

K-Number: K072830 · 2007-12-04

ApplicantPentron Clinical Technologies
Decision Date2007-12-04
Product CodeDYH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RM BOND, MODEL J032 is the device name listed in this FDA 510(k) record. The listed applicant is Pentron Clinical Technologies. It received FDA 510(k) clearance on 2007-12-04 under 510(k) number K072830. The device is classified under product code DYH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RM BOND, MODEL J032?

RM BOND, MODEL J032 is a medical device that received FDA 510(k) clearance on 2007-12-04. The listed applicant is Pentron Clinical Technologies. The 510(k) number is K072830.

When did RM BOND, MODEL J032 receive FDA 510(k) clearance?

RM BOND, MODEL J032 received FDA 510(k) clearance on 2007-12-04, under 510(k) number K072830.

Who is the listed applicant for RM BOND, MODEL J032?

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

What is the FDA product code for RM BOND, MODEL J032?

The FDA product code for RM BOND, MODEL J032 is DYH.

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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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