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FDA 510(k)

SURGICAL LIGHT - CHALLENGE 22 SERIES

K-Number: K761018 · 1977-01-26

ApplicantAmsco Co.
Decision Date1977-01-26
Product CodeFQP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGICAL LIGHT - CHALLENGE 22 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Amsco Co.. It received FDA 510(k) clearance on 1977-01-26 under 510(k) number K761018. The device is classified under product code FQP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL LIGHT - CHALLENGE 22 SERIES?

SURGICAL LIGHT - CHALLENGE 22 SERIES is a medical device that received FDA 510(k) clearance on 1977-01-26. The listed applicant is Amsco Co.. The 510(k) number is K761018.

When did SURGICAL LIGHT - CHALLENGE 22 SERIES receive FDA 510(k) clearance?

SURGICAL LIGHT - CHALLENGE 22 SERIES received FDA 510(k) clearance on 1977-01-26, under 510(k) number K761018.

Who is the listed applicant for SURGICAL LIGHT - CHALLENGE 22 SERIES?

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

What is the FDA product code for SURGICAL LIGHT - CHALLENGE 22 SERIES?

The FDA product code for SURGICAL LIGHT - CHALLENGE 22 SERIES is FQP.

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Other records listing Amsco Co. 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.

K912471EAGLE 3000 SDSK854922AMSCO POLARIS SLK833187HALL OSTEONK832945EAGLE 2000 STERILIZER SERIES GAS/AERAK832188HALL RECIPROCATORK832187HALL OSCILLATOR

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Related Devices (Code: FQP)

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.

K001223ACULUX, MODEL AX3001, AX3002AculuxK993314SYNTHES LIGHT GUIDESynthes (Usa)K781581SURGICAL LIGHT 22 SERIESAmerican Sterilizer Co.K770812HANDLES, LIGHT, SURGICAL, STEOILESybron Corp.

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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