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FDA 510(k)

SENSOMAT SIDEARM ADAPTER

K-Number: K790597 · 1979-07-10

ApplicantBiochem International, Inc.
Decision Date1979-07-10
Product CodeKGZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SENSOMAT SIDEARM ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Biochem International, Inc.. It received FDA 510(k) clearance on 1979-07-10 under 510(k) number K790597. The device is classified under product code KGZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SENSOMAT SIDEARM ADAPTER?

SENSOMAT SIDEARM ADAPTER is a medical device that received FDA 510(k) clearance on 1979-07-10. The listed applicant is Biochem International, Inc.. The 510(k) number is K790597.

When did SENSOMAT SIDEARM ADAPTER receive FDA 510(k) clearance?

SENSOMAT SIDEARM ADAPTER received FDA 510(k) clearance on 1979-07-10, under 510(k) number K790597.

Who is the listed applicant for SENSOMAT SIDEARM ADAPTER?

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

What is the FDA product code for SENSOMAT SIDEARM ADAPTER?

The FDA product code for SENSOMAT SIDEARM ADAPTER is KGZ.

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Other records listing Biochem International, 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.

K920083BIOCHEM MODEL 3302 NEWOX2 OXIMETERK9323898100 ANESTHETIC AGENT MONITORK921388BIOCHEM 9100 MULTIGAS MONITOR IBP MODULEK920082BIOCHEM MODEL 3301 NEWOX1 OXIMETERK911351BIOCHEM 9100 MULTIGAS MONITOR TEMP/FIO1 MOD,NIBPK910381BIOCHEM TEMPERATURE/ FIO2 MODULE

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Related Devices (Code: KGZ)

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.

K022306AART SILICONE TUBINGAesthetic and Reconstructive Technologies, Inc.K974295BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBINGByron MedicalK973183WOUND DRAINAGE HOLDERR & D Medical Products, Inc.K955433DURALASTIC SILICONE TUBINGAllied Biomedical Corp.K942315NAVARRE PERCUTANEOUS ACCESS SETNavarre Biomedical , Ltd.K896087PALESTRANT IRRIGATION AND DRAINAGE SETNorth American Instrument 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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