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FDA 510(k)

SSS, MODEL 1072001 (STANDARD 4-HOLE MODEL) & 1072002 (STANDARD 2-HOLE MODEL)

K-Number: K032995 · 2003-11-20

ApplicantMicron Corp.
Decision Date2003-11-20
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SSS, MODEL 1072001 (STANDARD 4-HOLE MODEL) & 1072002 (STANDARD 2-HOLE MODEL) is the device name listed in this FDA 510(k) record. The listed applicant is Micron Corp.. It received FDA 510(k) clearance on 2003-11-20 under 510(k) number K032995. The device is classified under product code ELC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SSS, MODEL 1072001 (STANDARD 4-HOLE MODEL) & 1072002 (STANDARD 2-HOLE MODEL)?

SSS, MODEL 1072001 (STANDARD 4-HOLE MODEL) & 1072002 (STANDARD 2-HOLE MODEL) is a medical device that received FDA 510(k) clearance on 2003-11-20. The listed applicant is Micron Corp.. The 510(k) number is K032995.

When did SSS, MODEL 1072001 (STANDARD 4-HOLE MODEL) & 1072002 (STANDARD 2-HOLE MODEL) receive FDA 510(k) clearance?

SSS, MODEL 1072001 (STANDARD 4-HOLE MODEL) & 1072002 (STANDARD 2-HOLE MODEL) received FDA 510(k) clearance on 2003-11-20, under 510(k) number K032995.

Who is the listed applicant for SSS, MODEL 1072001 (STANDARD 4-HOLE MODEL) & 1072002 (STANDARD 2-HOLE MODEL)?

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

What is the FDA product code for SSS, MODEL 1072001 (STANDARD 4-HOLE MODEL) & 1072002 (STANDARD 2-HOLE MODEL)?

The FDA product code for SSS, MODEL 1072001 (STANDARD 4-HOLE MODEL) & 1072002 (STANDARD 2-HOLE MODEL) is ELC.

Related Clinical Trials

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Other records listing Micron Corp. 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.

K991239VIP 60 (2H), MODEL 115-000-1, VIP 60 (4H), MODEL 115-000-2

Related Devices (Code: ELC)

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

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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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