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FDA 510(k)

SHILEY EQUIPMENT SUPPORT CARTS ESC-002 & ESCB-02

K-Number: K892446 · 1989-07-14

ApplicantShiley, Inc.
Decision Date1989-07-14
Product CodeKRD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SHILEY EQUIPMENT SUPPORT CARTS ESC-002 & ESCB-02 is the device name listed in this FDA 510(k) record. The listed applicant is Shiley, Inc.. It received FDA 510(k) clearance on 1989-07-14 under 510(k) number K892446. The device is classified under product code KRD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHILEY EQUIPMENT SUPPORT CARTS ESC-002 & ESCB-02?

SHILEY EQUIPMENT SUPPORT CARTS ESC-002 & ESCB-02 is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is Shiley, Inc.. The 510(k) number is K892446.

When did SHILEY EQUIPMENT SUPPORT CARTS ESC-002 & ESCB-02 receive FDA 510(k) clearance?

SHILEY EQUIPMENT SUPPORT CARTS ESC-002 & ESCB-02 received FDA 510(k) clearance on 1989-07-14, under 510(k) number K892446.

Who is the listed applicant for SHILEY EQUIPMENT SUPPORT CARTS ESC-002 & ESCB-02?

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

What is the FDA product code for SHILEY EQUIPMENT SUPPORT CARTS ESC-002 & ESCB-02?

The FDA product code for SHILEY EQUIPMENT SUPPORT CARTS ESC-002 & ESCB-02 is KRD.

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Other records listing Shiley, Inc. as applicant

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Related Devices (Code: KRD)

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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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