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FDA 510(k)

SIEMENS SIRECUST MODELS 403P,403-2P & 403N

K-Number: K855096 · 1986-07-15

ApplicantAnalogic Corp.
Decision Date1986-07-15
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIEMENS SIRECUST MODELS 403P,403-2P & 403N is the device name listed in this FDA 510(k) record. The listed applicant is Analogic Corp.. It received FDA 510(k) clearance on 1986-07-15 under 510(k) number K855096. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS SIRECUST MODELS 403P,403-2P & 403N?

SIEMENS SIRECUST MODELS 403P,403-2P & 403N is a medical device that received FDA 510(k) clearance on 1986-07-15. The listed applicant is Analogic Corp.. The 510(k) number is K855096.

When did SIEMENS SIRECUST MODELS 403P,403-2P & 403N receive FDA 510(k) clearance?

SIEMENS SIRECUST MODELS 403P,403-2P & 403N received FDA 510(k) clearance on 1986-07-15, under 510(k) number K855096.

Who is the listed applicant for SIEMENS SIRECUST MODELS 403P,403-2P & 403N?

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

What is the FDA product code for SIEMENS SIRECUST MODELS 403P,403-2P & 403N?

The FDA product code for SIEMENS SIRECUST MODELS 403P,403-2P & 403N is DPS.

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Other records listing Analogic 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.

K071430SYNERAD OMNI, MODELS AN6255 AND AN6265K052447SYNERAD IMPACT 60, SYNERAD IMPACT 72 AND ANALOGIC AMS1600K050919LIFEGARD II FAMILY MULTI-FUNCTION PATIENT MONITOR, MODELS AN4320, AN4320P, AN4321P, AN4322P & AN3423PK043025SYNERAD OMNI, DIGITAL X-RAY SYSTEM, MODEL AN6250K041434C3 AND LIFEGARD ICG IMPEDANCE CARDIOGRAPHY MONITORSK041376C1 SERIES PATIENT MONITOR, MODELS 863051, 863052, 863053, 863054; OPTIONAL PRINTER FOR CI, MODEL M3925A

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Related Devices (Code: DPS)

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.

K254255S-Patch CardioAIWellysis Corp.K252463SE-1202 Series Electrocardiograph (Model: SE-1202, SE-1202E)Edan Instruments, Inc.K251670MAC 7 Resting ECG Analysis SystemGe Medical Systems Information Technologies, Inc.K252361AccurECG Analysis System (v2.0)Accurkardia, Inc.K252474Withings BeamO (SCT02)WithingsK250569Cardiologs Holter PlatformPhilips France Commercial

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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