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FDA 510(k)

RADIATION THERAPY TREAT. PLAN. SYS.

K-Number: K780278 · 1978-03-02

ApplicantPfizer Medical Systems, Inc.
Decision Date1978-03-02
Product CodeJAD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RADIATION THERAPY TREAT. PLAN. SYS. 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 1978-03-02 under 510(k) number K780278. The device is classified under product code JAD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADIATION THERAPY TREAT. PLAN. SYS.?

RADIATION THERAPY TREAT. PLAN. SYS. is a medical device that received FDA 510(k) clearance on 1978-03-02. The listed applicant is Pfizer Medical Systems, Inc.. The 510(k) number is K780278.

When did RADIATION THERAPY TREAT. PLAN. SYS. receive FDA 510(k) clearance?

RADIATION THERAPY TREAT. PLAN. SYS. received FDA 510(k) clearance on 1978-03-02, under 510(k) number K780278.

Who is the listed applicant for RADIATION THERAPY TREAT. PLAN. SYS.?

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 RADIATION THERAPY TREAT. PLAN. SYS.?

The FDA product code for RADIATION THERAPY TREAT. PLAN. SYS. is JAD.

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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 SCANNERK802530PFIZONIC 250 ULTRASOUND SCANNERK802529PFIZONIC 100 ULTRASOUND SCANNERK802532PFIZONIC 300 ULTRASOUND SCANNER

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Related Devices (Code: JAD)

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.

K250692GentleBeam (GB1000)Voxel Ray Solutions, LLCK241174INTRABEAM (700); And accessories (INTRABEAM SMART Stand, INTRABEAM SMART Spherical Applicator, INTRABEAM Spherical Sizer Set, INTRABEAM Needle Applicator)Carl Zeiss Meditec, AGK230611X80 / RADiant / PhotoElectric Therapy System (RADiant Aura)Xstrahl, Ltd.K213942EsteyaNucletron B.V.K190255Sensus Healthcare TVM Balloon ApplicatorSensus Healthcare, Inc.K182641Sensus IORT SystemSensus Healthcare, 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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