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FDA 510(k)

LCR GENERATOR

K-Number: K931998 · 1993-07-27

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1993-07-27
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LCR GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems (Cleveland), Inc.. It received FDA 510(k) clearance on 1993-07-27 under 510(k) number K931998. The device is classified under product code IZO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LCR GENERATOR?

LCR GENERATOR is a medical device that received FDA 510(k) clearance on 1993-07-27. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K931998.

When did LCR GENERATOR receive FDA 510(k) clearance?

LCR GENERATOR received FDA 510(k) clearance on 1993-07-27, under 510(k) number K931998.

Who is the listed applicant for LCR GENERATOR?

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

What is the FDA product code for LCR GENERATOR?

The FDA product code for LCR GENERATOR is IZO.

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Other records listing Philips Medical Systems (Cleveland), Inc. as applicant

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Related Devices (Code: IZO)

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.

K954666MPH50, MPH65, AND MPH80GE Medical SystemsK953582HFX350, 30KW, 300MA, 1 OR 3 PHASE RADIOGRAPHIC & FLUOROSCOPIC X-RAY GENERATORVarian Canada, Inc.K953831N 800 HFNucletron-Oldelft Corp.K952822SHIMADZU X-RAY HIGH VILTAGE GENERATOR AHD150GShimadzu Corp.K952265MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATORControl-X, Inc.K950883POLYDOROS SX 65 AND 80Siemens Medical Solutions USA, 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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