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FDA 510(k)

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

K-Number: K991239 · 1999-10-18

ApplicantMicron Corp.
Decision Date1999-10-18
Product CodeELC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VIP 60 (2H), MODEL 115-000-1, VIP 60 (4H), MODEL 115-000-2 is the device name listed in this FDA 510(k) record. The listed applicant is Micron Corp.. It received FDA 510(k) clearance on 1999-10-18 under 510(k) number K991239. 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 VIP 60 (2H), MODEL 115-000-1, VIP 60 (4H), MODEL 115-000-2?

VIP 60 (2H), MODEL 115-000-1, VIP 60 (4H), MODEL 115-000-2 is a medical device that received FDA 510(k) clearance on 1999-10-18. The listed applicant is Micron Corp.. The 510(k) number is K991239.

When did VIP 60 (2H), MODEL 115-000-1, VIP 60 (4H), MODEL 115-000-2 receive FDA 510(k) clearance?

VIP 60 (2H), MODEL 115-000-1, VIP 60 (4H), MODEL 115-000-2 received FDA 510(k) clearance on 1999-10-18, under 510(k) number K991239.

Who is the listed applicant for VIP 60 (2H), MODEL 115-000-1, VIP 60 (4H), MODEL 115-000-2?

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

The FDA product code for VIP 60 (2H), MODEL 115-000-1, VIP 60 (4H), MODEL 115-000-2 is ELC.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K032995SSS, MODEL 1072001 (STANDARD 4-HOLE MODEL) & 1072002 (STANDARD 2-HOLE MODEL)

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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