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FDA 510(k)

THE PLACER

K-Number: K811582 · 1981-07-28

ApplicantCavitron Corp.
Decision Date1981-07-28
Product CodeEID
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

THE PLACER is the device name listed in this FDA 510(k) record. The listed applicant is Cavitron Corp.. It received FDA 510(k) clearance on 1981-07-28 under 510(k) number K811582. 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 THE PLACER?

THE PLACER is a medical device that received FDA 510(k) clearance on 1981-07-28. The listed applicant is Cavitron Corp.. The 510(k) number is K811582.

When did THE PLACER receive FDA 510(k) clearance?

THE PLACER received FDA 510(k) clearance on 1981-07-28, under 510(k) number K811582.

Who is the listed applicant for THE PLACER?

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

What is the FDA product code for THE PLACER?

The FDA product code for THE PLACER is EID.

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Other records listing Cavitron Corp. 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.

K810207MINOR SURGERY LIGHTK802928SPIROMETRIC COMPUTER #SC-10K801623CAVITRON ULTRASONIC SURG. ASPIR. CUSAK801877SLIT LAMP ATTACHMENTK800869MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALAK800722AUTO-FIELD D AUTOMATED VISUAL DETECTOR

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Related Devices (Code: EID)

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.

K941431BONE GRAFT DELIVERY SYRINGESBio-Interfaces, Inc.K913974ACCESS IMPRESSION BARRELCentrix, Inc.K873153CAULK'S VPS CARTRIDGE SYSTEMDentsply Intl.K871937IMPRESSION SYRINGEDentsply Intl.K863998COLTENE JET-MIXERColtene, Inc.K853282CENTRIX RIBBON TUBESCentrix, Inc.

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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