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FDA 510(k)

MULTI-FORMAT SFD MODEL 1720

K-Number: K800554 · 1980-04-10

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1980-04-10
Product CodeIXL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MULTI-FORMAT SFD MODEL 1720 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 1980-04-10 under 510(k) number K800554. The device is classified under product code IXL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-FORMAT SFD MODEL 1720?

MULTI-FORMAT SFD MODEL 1720 is a medical device that received FDA 510(k) clearance on 1980-04-10. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K800554.

When did MULTI-FORMAT SFD MODEL 1720 receive FDA 510(k) clearance?

MULTI-FORMAT SFD MODEL 1720 received FDA 510(k) clearance on 1980-04-10, under 510(k) number K800554.

Who is the listed applicant for MULTI-FORMAT SFD MODEL 1720?

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 MULTI-FORMAT SFD MODEL 1720?

The FDA product code for MULTI-FORMAT SFD MODEL 1720 is IXL.

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Related Devices (Code: IXL)

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.

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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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