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FDA 510(k)

CUTTERSIL XL

K-Number: K910166 · 1991-06-06

ApplicantHeraeus Kulzer, Inc.
Decision Date1991-06-06
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CUTTERSIL XL is the device name listed in this FDA 510(k) record. The listed applicant is Heraeus Kulzer, Inc.. It received FDA 510(k) clearance on 1991-06-06 under 510(k) number K910166. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUTTERSIL XL?

CUTTERSIL XL is a medical device that received FDA 510(k) clearance on 1991-06-06. The listed applicant is Heraeus Kulzer, Inc.. The 510(k) number is K910166.

When did CUTTERSIL XL receive FDA 510(k) clearance?

CUTTERSIL XL received FDA 510(k) clearance on 1991-06-06, under 510(k) number K910166.

Who is the listed applicant for CUTTERSIL XL?

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

What is the FDA product code for CUTTERSIL XL?

The FDA product code for CUTTERSIL XL is ELW.

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Other records listing Heraeus Kulzer, 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.

K091494FLEXITIME FLOWK063062HKBOND 2006K060994MONDIALK052543HERACERAM ZIRKONIAK043504PALAIMPACTK043295VERSYO.DIRECT

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Related Devices (Code: ELW)

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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