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FDA 510(k)

BONETRAP

K-Number: K980049 · 1998-08-11

ApplicantBladhs Plast AB
Decision Date1998-08-11
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BONETRAP is the device name listed in this FDA 510(k) record. The listed applicant is Bladhs Plast AB. It received FDA 510(k) clearance on 1998-08-11 under 510(k) number K980049. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BONETRAP?

BONETRAP is a medical device that received FDA 510(k) clearance on 1998-08-11. The listed applicant is Bladhs Plast AB. The 510(k) number is K980049.

When did BONETRAP receive FDA 510(k) clearance?

BONETRAP received FDA 510(k) clearance on 1998-08-11, under 510(k) number K980049.

Who is the listed applicant for BONETRAP?

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

What is the FDA product code for BONETRAP?

The FDA product code for BONETRAP is EIA.

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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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