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FDA 510(k)

CAULK'S VPS CARTRIDGE SYSTEM

K-Number: K873153 · 1987-09-16

ApplicantDentsply Intl.
Decision Date1987-09-16
Product CodeEID
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CAULK'S VPS CARTRIDGE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1987-09-16 under 510(k) number K873153. The device is classified under product code EID. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAULK'S VPS CARTRIDGE SYSTEM?

CAULK'S VPS CARTRIDGE SYSTEM is a medical device that received FDA 510(k) clearance on 1987-09-16. The listed applicant is Dentsply Intl.. The 510(k) number is K873153.

When did CAULK'S VPS CARTRIDGE SYSTEM receive FDA 510(k) clearance?

CAULK'S VPS CARTRIDGE SYSTEM received FDA 510(k) clearance on 1987-09-16, under 510(k) number K873153.

Who is the listed applicant for CAULK'S VPS CARTRIDGE SYSTEM?

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

What is the FDA product code for CAULK'S VPS CARTRIDGE SYSTEM?

The FDA product code for CAULK'S VPS CARTRIDGE SYSTEM is EID.

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Related Devices (Code: EID)

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K941431BONE GRAFT DELIVERY SYRINGESBio-Interfaces, Inc.K913974ACCESS IMPRESSION BARRELCentrix, Inc.K871937IMPRESSION SYRINGEDentsply Intl.K863998COLTENE JET-MIXERColtene, Inc.K853282CENTRIX RIBBON TUBESCentrix, Inc.K851386UNITEK DISPOSABLE IMPRESSION SYRINGEUnitek Corp.

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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