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FDA 510(k)

POLYTRON MODELS 1001, 1002 AND 1004

K-Number: K870821 · 1987-07-01

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1987-07-01
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

POLYTRON MODELS 1001, 1002 AND 1004 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1987-07-01 under 510(k) number K870821. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POLYTRON MODELS 1001, 1002 AND 1004?

POLYTRON MODELS 1001, 1002 AND 1004 is a medical device that received FDA 510(k) clearance on 1987-07-01. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K870821.

When did POLYTRON MODELS 1001, 1002 AND 1004 receive FDA 510(k) clearance?

POLYTRON MODELS 1001, 1002 AND 1004 received FDA 510(k) clearance on 1987-07-01, under 510(k) number K870821.

Who is the listed applicant for POLYTRON MODELS 1001, 1002 AND 1004?

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

What is the FDA product code for POLYTRON MODELS 1001, 1002 AND 1004?

The FDA product code for POLYTRON MODELS 1001, 1002 AND 1004 is LLZ.

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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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