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FDA 510(k)

PHILIPS RT250 COLLIMATOR (PK8050)

K-Number: K885126 · 1989-06-01

ApplicantPerkins Mfg. Co.
Decision Date1989-06-01
Product CodeKQA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PHILIPS RT250 COLLIMATOR (PK8050) is the device name listed in this FDA 510(k) record. The listed applicant is Perkins Mfg. Co.. It received FDA 510(k) clearance on 1989-06-01 under 510(k) number K885126. The device is classified under product code KQA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHILIPS RT250 COLLIMATOR (PK8050)?

PHILIPS RT250 COLLIMATOR (PK8050) is a medical device that received FDA 510(k) clearance on 1989-06-01. The listed applicant is Perkins Mfg. Co.. The 510(k) number is K885126.

When did PHILIPS RT250 COLLIMATOR (PK8050) receive FDA 510(k) clearance?

PHILIPS RT250 COLLIMATOR (PK8050) received FDA 510(k) clearance on 1989-06-01, under 510(k) number K885126.

Who is the listed applicant for PHILIPS RT250 COLLIMATOR (PK8050)?

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

What is the FDA product code for PHILIPS RT250 COLLIMATOR (PK8050)?

The FDA product code for PHILIPS RT250 COLLIMATOR (PK8050) is KQA.

Related Clinical Trials

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Other records listing Perkins Mfg. Co. 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.

K972136TV MONITOR (P12/17)K954222VIDEO ENHANCEMENT UNITK926348SC1000 SCAN CONVERTERK920550DISPLAY PROCESSOR - MODEL IDP5100K915232GRUNDIG ELECTRONICS VARIOUS MODELSK910384VIDEO ANNOTATOR MODEL PK2310

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Related Devices (Code: KQA)

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.

K914784PAPILLION PROCTOSCOPEOldelft Corp. of AmericaK844180THE MCP-70-SE SYSTEMEllis Pharmaceutical Consulting, Inc.K790168COLLIMATOR, BILATERIALCmsi

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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