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FDA 510(k)

ULTRABLADE

K-Number: K921167 · 1992-07-30

ApplicantMicron Technology, Inc.
Decision Date1992-07-30
Product CodeGDX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ULTRABLADE is the device name listed in this FDA 510(k) record. The listed applicant is Micron Technology, Inc.. It received FDA 510(k) clearance on 1992-07-30 under 510(k) number K921167. The device is classified under product code GDX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRABLADE?

ULTRABLADE is a medical device that received FDA 510(k) clearance on 1992-07-30. The listed applicant is Micron Technology, Inc.. The 510(k) number is K921167.

When did ULTRABLADE receive FDA 510(k) clearance?

ULTRABLADE received FDA 510(k) clearance on 1992-07-30, under 510(k) number K921167.

Who is the listed applicant for ULTRABLADE?

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

What is the FDA product code for ULTRABLADE?

The FDA product code for ULTRABLADE is GDX.

Related Clinical Trials

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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Other records listing Micron Technology, 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.

K863121PEAK OVULATION PREDICTOR

Related Devices (Code: GDX)

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.

K923689SURGISTAR BLADESSurgistar, Inc.K914086ICAN CYLINDRICAL SPONGESIcn Pharmaceuticals, Inc.K904505CCI CORNEAL SCARIFIERBuckman Co., Inc.K9053801-CUT ACL GRAFT KNIFEDepuy, Inc.K895682VESSEL LOOPSApplied Medical TechnologiesK893033MINI-DIAMOND KNIFEL.A.B. Instruments

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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