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FDA 510(k)

EEC-1 PACKAGE

K-Number: K923819 · 1992-11-06

ApplicantMed Labs, Inc.
Decision Date1992-11-06
Product CodeILQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EEC-1 PACKAGE is the device name listed in this FDA 510(k) record. The listed applicant is Med Labs, Inc.. It received FDA 510(k) clearance on 1992-11-06 under 510(k) number K923819. The device is classified under product code ILQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EEC-1 PACKAGE?

EEC-1 PACKAGE is a medical device that received FDA 510(k) clearance on 1992-11-06. The listed applicant is Med Labs, Inc.. The 510(k) number is K923819.

When did EEC-1 PACKAGE receive FDA 510(k) clearance?

EEC-1 PACKAGE received FDA 510(k) clearance on 1992-11-06, under 510(k) number K923819.

Who is the listed applicant for EEC-1 PACKAGE?

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

What is the FDA product code for EEC-1 PACKAGE?

The FDA product code for EEC-1 PACKAGE is ILQ.

Related Clinical Trials

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Other records listing Med Labs, 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.

K960457ELECTRONIC MUSCLE STIMULATOR MODEL EMS-1C/EMS-2CK935981MLT-2K903652SCAN COM AND SCAN COM P (TENTATIVE)

Related Devices (Code: ILQ)

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.

K162817Noddle(TM)Iowa Adaptive Technologies, Inc. Dba Voxello, Inc.K943035P.A.T. SYSTEMMathews Assoc., Inc.K930044COMFORT KEYBOARD SYSTEMHealth Care Keyboard Co., Inc.K931855LIGHTWRITERZygo Corp.K935244R & D BATTERIES, INC. PART NUMBER 5113R & D Batteries, Inc.K935981MLT-2Med Labs, Inc.

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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