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FDA 510(k)

LANCER - MODULAR POWER BASE

K-Number: K890723 · 1989-03-02

ApplicantEverest & Jennings, Inc.
Decision Date1989-03-02
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LANCER - MODULAR POWER BASE is the device name listed in this FDA 510(k) record. The listed applicant is Everest & Jennings, Inc.. It received FDA 510(k) clearance on 1989-03-02 under 510(k) number K890723. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LANCER - MODULAR POWER BASE?

LANCER - MODULAR POWER BASE is a medical device that received FDA 510(k) clearance on 1989-03-02. The listed applicant is Everest & Jennings, Inc.. The 510(k) number is K890723.

When did LANCER - MODULAR POWER BASE receive FDA 510(k) clearance?

LANCER - MODULAR POWER BASE received FDA 510(k) clearance on 1989-03-02, under 510(k) number K890723.

Who is the listed applicant for LANCER - MODULAR POWER BASE?

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

What is the FDA product code for LANCER - MODULAR POWER BASE?

The FDA product code for LANCER - MODULAR POWER BASE is ITI.

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Other records listing Everest & Jennings, 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.

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Related Devices (Code: ITI)

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

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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