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FDA 510(k)

PHILIPS NICOL COLLIMATOR FAMILY

K-Number: K990423 · 1999-03-15

Decision Date1999-03-15
Product CodeIZW
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PHILIPS NICOL COLLIMATOR FAMILY is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems, Inc.. It received FDA 510(k) clearance on 1999-03-15 under 510(k) number K990423. The device is classified under product code IZW. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHILIPS NICOL COLLIMATOR FAMILY?

PHILIPS NICOL COLLIMATOR FAMILY is a medical device that received FDA 510(k) clearance on 1999-03-15. The listed applicant is Philips Medical Systems, Inc.. The 510(k) number is K990423.

When did PHILIPS NICOL COLLIMATOR FAMILY receive FDA 510(k) clearance?

PHILIPS NICOL COLLIMATOR FAMILY received FDA 510(k) clearance on 1999-03-15, under 510(k) number K990423.

Who is the listed applicant for PHILIPS NICOL COLLIMATOR FAMILY?

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

What is the FDA product code for PHILIPS NICOL COLLIMATOR FAMILY?

The FDA product code for PHILIPS NICOL COLLIMATOR FAMILY is IZW.

Related Clinical Trials

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.

Other records listing Philips 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.

View all 111 devices →

Related Devices (Code: IZW)

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.

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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