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FDA 510(k)

ENCORE SS-B

K-Number: K922340 · 1992-10-16

ApplicantClark Laboratories, Inc.
Decision Date1992-10-16
Product CodeLLL
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

ENCORE SS-B is the device name listed in this FDA 510(k) record. The listed applicant is Clark Laboratories, Inc.. It received FDA 510(k) clearance on 1992-10-16 under 510(k) number K922340. The device is classified under product code LLL. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENCORE SS-B?

ENCORE SS-B is a medical device that received FDA 510(k) clearance on 1992-10-16. The listed applicant is Clark Laboratories, Inc.. The 510(k) number is K922340.

When did ENCORE SS-B receive FDA 510(k) clearance?

ENCORE SS-B received FDA 510(k) clearance on 1992-10-16, under 510(k) number K922340.

Who is the listed applicant for ENCORE SS-B?

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

What is the FDA product code for ENCORE SS-B?

The FDA product code for ENCORE SS-B is LLL.

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Other records listing Clark Laboratories, 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: LLL)

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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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