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FDA 510(k)

PLP EVACUATION CONTROL SYSTEM 1 MICRO (ECS.1UM)

K-Number: K912853 · 1991-08-20

Decision Date1991-08-20
Product CodeFYD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PLP EVACUATION CONTROL SYSTEM 1 MICRO (ECS.1UM) is the device name listed in this FDA 510(k) record. The listed applicant is Precision Laser Products, Inc.. It received FDA 510(k) clearance on 1991-08-20 under 510(k) number K912853. The device is classified under product code FYD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLP EVACUATION CONTROL SYSTEM 1 MICRO (ECS.1UM)?

PLP EVACUATION CONTROL SYSTEM 1 MICRO (ECS.1UM) is a medical device that received FDA 510(k) clearance on 1991-08-20. The listed applicant is Precision Laser Products, Inc.. The 510(k) number is K912853.

When did PLP EVACUATION CONTROL SYSTEM 1 MICRO (ECS.1UM) receive FDA 510(k) clearance?

PLP EVACUATION CONTROL SYSTEM 1 MICRO (ECS.1UM) received FDA 510(k) clearance on 1991-08-20, under 510(k) number K912853.

Who is the listed applicant for PLP EVACUATION CONTROL SYSTEM 1 MICRO (ECS.1UM)?

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

What is the FDA product code for PLP EVACUATION CONTROL SYSTEM 1 MICRO (ECS.1UM)?

The FDA product code for PLP EVACUATION CONTROL SYSTEM 1 MICRO (ECS.1UM) is FYD.

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.

Other records listing Precision Laser Products, 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.

Related Devices (Code: FYD)

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.

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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