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FDA 510(k)

SARNO SINGLE POLE MAST

K-Number: K790192 · 1979-02-08

ApplicantSames, Inc.
Decision Date1979-02-08
Product CodeKRI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SARNO SINGLE POLE MAST is the device name listed in this FDA 510(k) record. The listed applicant is Sames, Inc.. It received FDA 510(k) clearance on 1979-02-08 under 510(k) number K790192. The device is classified under product code KRI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SARNO SINGLE POLE MAST?

SARNO SINGLE POLE MAST is a medical device that received FDA 510(k) clearance on 1979-02-08. The listed applicant is Sames, Inc.. The 510(k) number is K790192.

When did SARNO SINGLE POLE MAST receive FDA 510(k) clearance?

SARNO SINGLE POLE MAST received FDA 510(k) clearance on 1979-02-08, under 510(k) number K790192.

Who is the listed applicant for SARNO SINGLE POLE MAST?

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

What is the FDA product code for SARNO SINGLE POLE MAST?

The FDA product code for SARNO SINGLE POLE MAST is KRI.

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Related Devices (Code: KRI)

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.

K0203653TM MYOCARDIAL NEEDLE-TEMPERATURE PROBE3t Medical Systems, LLCK992635INTERFACE MODULE IDDDStoeckert InstrumenteK990512STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTSStoeckert InstrumenteK934782AMMEX TUBING ORGANIZERAmmex Cardiopulmonary Corp.K926233CARDIO2 CYCLEErgometrix, Inc.K922404TUBE GRIPGeorgia Medical Products, 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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