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FDA 510(k)

EASE (MODIFICATION TO)

K-Number: K771403 · 1977-08-22

ApplicantL.D. Caulk Co.
Decision Date1977-08-22
Product CodeEJJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EASE (MODIFICATION TO) is the device name listed in this FDA 510(k) record. The listed applicant is L.D. Caulk Co.. It received FDA 510(k) clearance on 1977-08-22 under 510(k) number K771403. The device is classified under product code EJJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EASE (MODIFICATION TO)?

EASE (MODIFICATION TO) is a medical device that received FDA 510(k) clearance on 1977-08-22. The listed applicant is L.D. Caulk Co.. The 510(k) number is K771403.

When did EASE (MODIFICATION TO) receive FDA 510(k) clearance?

EASE (MODIFICATION TO) received FDA 510(k) clearance on 1977-08-22, under 510(k) number K771403.

Who is the listed applicant for EASE (MODIFICATION TO)?

The FDA 510(k) record lists L.D. Caulk Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EASE (MODIFICATION TO)?

The FDA product code for EASE (MODIFICATION TO) is EJJ.

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Other records listing L.D. Caulk Co. 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.

K802262COMPOSITE RESTORATIVEK801690VALIANTK790586CHEMBONDK790585FINESSEK780560DENTAL AMALGAMATORK780384IMPROVED DYCAL

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Related Devices (Code: EJJ)

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.

K053114SILVERFILDunia Perwira Manufacturing Sdn. Bhd.K051010SECURALLOY, SEPTALLOY NG 50 AND SEPTALLOY NG 70SeptodontK033434BESTALOYWe Dong Myung Dental Industrial Co., Ltd.K032152BENCO ADMIXSouthern Dental Industries, Inc.K031658BENCO SPHERICALSouthern Dental Industries, Inc.K020452HIGH SILVER CONVENTIONALAb Ardent

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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