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FDA 510(k)

PFIZONIC 250 ULTRASOUND SCANNER

K-Number: K802530 · 1980-12-18

ApplicantPfizer Medical Systems, Inc.
Decision Date1980-12-18
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PFIZONIC 250 ULTRASOUND SCANNER 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 1980-12-18 under 510(k) number K802530. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PFIZONIC 250 ULTRASOUND SCANNER?

PFIZONIC 250 ULTRASOUND SCANNER is a medical device that received FDA 510(k) clearance on 1980-12-18. The listed applicant is Pfizer Medical Systems, Inc.. The 510(k) number is K802530.

When did PFIZONIC 250 ULTRASOUND SCANNER receive FDA 510(k) clearance?

PFIZONIC 250 ULTRASOUND SCANNER received FDA 510(k) clearance on 1980-12-18, under 510(k) number K802530.

Who is the listed applicant for PFIZONIC 250 ULTRASOUND SCANNER?

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 PFIZONIC 250 ULTRASOUND SCANNER?

The FDA product code for PFIZONIC 250 ULTRASOUND SCANNER is IYO.

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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.

K803032PFIZER PZ-SLM RAD. THERAPY TRTMT. SIMUL.K802531PFIZONIC 200 ULTRASOUND SCANNERK802528PFIZONIC 150 ULTRASOUND SCANNERK802529PFIZONIC 100 ULTRASOUND SCANNERK802532PFIZONIC 300 ULTRASOUND SCANNERK801446PFIZER PZ-CT SCANNER

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Related Devices (Code: IYO)

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.

K260313MD-6000S Bladder ScannerMEDA Co., Ltd.K253452Accuro 3SRivanna Medical, Inc.K260190ARTHURROPCA ApSK252237EdgeFlow UW20Edgecare, Inc.K254021Accuro XVRivanna Medical, Inc.K253898QT Scanner 2000 Model AQT Imaging Holdings, 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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