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FDA 510(k)

37-702 AND 37-703 PC RAINBOW

K-Number: K900932 · 1990-12-05

ApplicantVictoreen, Inc.
Decision Date1990-12-05
Product CodeIYI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

37-702 AND 37-703 PC RAINBOW is the device name listed in this FDA 510(k) record. The listed applicant is Victoreen, Inc.. It received FDA 510(k) clearance on 1990-12-05 under 510(k) number K900932. The device is classified under product code IYI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 37-702 AND 37-703 PC RAINBOW?

37-702 AND 37-703 PC RAINBOW is a medical device that received FDA 510(k) clearance on 1990-12-05. The listed applicant is Victoreen, Inc.. The 510(k) number is K900932.

When did 37-702 AND 37-703 PC RAINBOW receive FDA 510(k) clearance?

37-702 AND 37-703 PC RAINBOW received FDA 510(k) clearance on 1990-12-05, under 510(k) number K900932.

Who is the listed applicant for 37-702 AND 37-703 PC RAINBOW?

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

What is the FDA product code for 37-702 AND 37-703 PC RAINBOW?

The FDA product code for 37-702 AND 37-703 PC RAINBOW is IYI.

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Other records listing Victoreen, 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.

K982937MODEL 580-006 RADIATION THERAPY IONIZATION CHAMBERK974112VACUDAP, MODEL 2000, 2001K973960MODEL 37-185K964952VERIDOSE V (FIVE), MODEL NUMBER 37-705K964785VERIDOSE DIODESK971382PRONE BREAST POSITIONING BOARD, MODEL #37-018

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Related Devices (Code: IYI)

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.

K914821CRS RADIATION BEAM SCANNERConsolidated Radiation Services, 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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