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FDA 510(k)

BILI-MIRROR MODEL BLM-1

K-Number: K093618 · 2010-04-23

ApplicantPhysician Engineered Products, Inc.
Decision Date2010-04-23
Product CodeLBI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BILI-MIRROR MODEL BLM-1 is the device name listed in this FDA 510(k) record. The listed applicant is Physician Engineered Products, Inc.. It received FDA 510(k) clearance on 2010-04-23 under 510(k) number K093618. The device is classified under product code LBI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BILI-MIRROR MODEL BLM-1?

BILI-MIRROR MODEL BLM-1 is a medical device that received FDA 510(k) clearance on 2010-04-23. The listed applicant is Physician Engineered Products, Inc.. The 510(k) number is K093618.

When did BILI-MIRROR MODEL BLM-1 receive FDA 510(k) clearance?

BILI-MIRROR MODEL BLM-1 received FDA 510(k) clearance on 2010-04-23, under 510(k) number K093618.

Who is the listed applicant for BILI-MIRROR MODEL BLM-1?

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

What is the FDA product code for BILI-MIRROR MODEL BLM-1?

The FDA product code for BILI-MIRROR MODEL BLM-1 is LBI.

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Other records listing Physician Engineered 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.

K110550BRIGHT EMBRACE MODEL SBL60K974830ULTRA BILI LIGHTK883818MODIFIED REFLUX REDUCERK882291RETROFIT BABY FACE SHIELD (RFS)K882278RESUSCITATION BAG CONTROLLER (RBC)K873700INSTITUTIONAL BILI LIGHT (IBL)

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Related Devices (Code: LBI)

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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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