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FDA 510(k)

ALLERGAN HUMPHREY A/B SCAN , MODEL 835

K-Number: K902582 · 1990-08-14

ApplicantAllergan Humphrey
Decision Date1990-08-14
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ALLERGAN HUMPHREY A/B SCAN , MODEL 835 is the device name listed in this FDA 510(k) record. The listed applicant is Allergan Humphrey. It received FDA 510(k) clearance on 1990-08-14 under 510(k) number K902582. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALLERGAN HUMPHREY A/B SCAN , MODEL 835?

ALLERGAN HUMPHREY A/B SCAN , MODEL 835 is a medical device that received FDA 510(k) clearance on 1990-08-14. The listed applicant is Allergan Humphrey. The 510(k) number is K902582.

When did ALLERGAN HUMPHREY A/B SCAN , MODEL 835 receive FDA 510(k) clearance?

ALLERGAN HUMPHREY A/B SCAN , MODEL 835 received FDA 510(k) clearance on 1990-08-14, under 510(k) number K902582.

Who is the listed applicant for ALLERGAN HUMPHREY A/B SCAN , MODEL 835?

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

What is the FDA product code for ALLERGAN HUMPHREY A/B SCAN , MODEL 835?

The FDA product code for ALLERGAN HUMPHREY A/B SCAN , MODEL 835 is IYO.

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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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Other records listing Allergan Humphrey 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.

K872312MODEL 3000 OPHTHALMIC SURGICAL SYSTEMK871611ALLERGAN HUMPHREY AUTO-REFRACTOR, MODELS 525 & 540

Related Devices (Code: IYO)

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.

K260313MD-6000S Bladder ScannerMEDA Co., Ltd.K253452Accuro 3SRivanna Medical, Inc.K260190ARTHURROPCA ApSK252237EdgeFlow UW20Edgecare, Inc.K254021Accuro XVRivanna Medical, Inc.K253898QT Scanner 2000 Model AQT Imaging Holdings, 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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