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FDA 510(k)

PFIZER PZ-SLM RAD. THERAPY TRTMT. SIMUL.

K-Number: K803032 · 1981-01-22

ApplicantPfizer Medical Systems, Inc.
Decision Date1981-01-22
Product CodeKPQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PFIZER PZ-SLM RAD. THERAPY TRTMT. SIMUL. is the device name listed in this FDA 510(k) record. The listed applicant is Pfizer Medical Systems, Inc.. It received FDA 510(k) clearance on 1981-01-22 under 510(k) number K803032. The device is classified under product code KPQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PFIZER PZ-SLM RAD. THERAPY TRTMT. SIMUL.?

PFIZER PZ-SLM RAD. THERAPY TRTMT. SIMUL. is a medical device that received FDA 510(k) clearance on 1981-01-22. The listed applicant is Pfizer Medical Systems, Inc.. The 510(k) number is K803032.

When did PFIZER PZ-SLM RAD. THERAPY TRTMT. SIMUL. receive FDA 510(k) clearance?

PFIZER PZ-SLM RAD. THERAPY TRTMT. SIMUL. received FDA 510(k) clearance on 1981-01-22, under 510(k) number K803032.

Who is the listed applicant for PFIZER PZ-SLM RAD. THERAPY TRTMT. SIMUL.?

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

What is the FDA product code for PFIZER PZ-SLM RAD. THERAPY TRTMT. SIMUL.?

The FDA product code for PFIZER PZ-SLM RAD. THERAPY TRTMT. SIMUL. is KPQ.

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Other records listing Pfizer Medical Systems, 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.

K802531PFIZONIC 200 ULTRASOUND SCANNERK802532PFIZONIC 300 ULTRASOUND SCANNERK802529PFIZONIC 100 ULTRASOUND SCANNERK802528PFIZONIC 150 ULTRASOUND SCANNERK802530PFIZONIC 250 ULTRASOUND SCANNERK801446PFIZER PZ-CT SCANNER

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Related Devices (Code: KPQ)

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.

K132045ADVANTAGESIM MD WITH CT ATLAS-BASED CONTOURING AND RE-PLANNING OPTIONSGe Hungary KftK101038RAD II SIMULATOR, RAD II KV IMAGER, DUAL RAD II KV IMAGERAcceletronics Digital Imaging, LLCK090706ONCENTRA SIMULATION 2.3Nucletron CorporationK083591IKOENGELO, VERSION 2Ikoetech, LLCK072445INTEGRATED BRACHYTHERAPY UNIT - DIGITALNucletron Corp.K061006IKOENGELOIkoetech, LLC

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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