FDA 510(k)

WIRE PASS DRILL BITS

K-Number: K880601 · 1988-05-06

ApplicantNuell Air Equipment & Hospital Supplies, Inc.

Decision Date1988-05-06

Product CodeHBE

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

WIRE PASS DRILL BITS is the device name listed in this FDA 510(k) record. The listed applicant is Nuell Air Equipment & Hospital Supplies, Inc.. It received FDA 510(k) clearance on 1988-05-06 under 510(k) number K880601. The device is classified under product code HBE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WIRE PASS DRILL BITS?

WIRE PASS DRILL BITS is a medical device that received FDA 510(k) clearance on 1988-05-06. The listed applicant is Nuell Air Equipment & Hospital Supplies, Inc.. The 510(k) number is K880601.

When did WIRE PASS DRILL BITS receive FDA 510(k) clearance?

WIRE PASS DRILL BITS received FDA 510(k) clearance on 1988-05-06, under 510(k) number K880601.

Who is the listed applicant for WIRE PASS DRILL BITS?

The FDA 510(k) record lists Nuell Air Equipment & Hospital Supplies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WIRE PASS DRILL BITS?

The FDA product code for WIRE PASS DRILL BITS is HBE.

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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.