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FDA 510(k)

KEELER MULTILASE 3000

K-Number: K942180 · 1994-11-22

ApplicantKeeler Instruments, Inc.
Decision Date1994-11-22
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

KEELER MULTILASE 3000 is the device name listed in this FDA 510(k) record. The listed applicant is Keeler Instruments, Inc.. It received FDA 510(k) clearance on 1994-11-22 under 510(k) number K942180. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KEELER MULTILASE 3000?

KEELER MULTILASE 3000 is a medical device that received FDA 510(k) clearance on 1994-11-22. The listed applicant is Keeler Instruments, Inc.. The 510(k) number is K942180.

When did KEELER MULTILASE 3000 receive FDA 510(k) clearance?

KEELER MULTILASE 3000 received FDA 510(k) clearance on 1994-11-22, under 510(k) number K942180.

Who is the listed applicant for KEELER MULTILASE 3000?

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

What is the FDA product code for KEELER MULTILASE 3000?

The FDA product code for KEELER MULTILASE 3000 is HQF.

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Other records listing Keeler Instruments, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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