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FDA 510(k)

SUCTION RETRACTORS

K-Number: K882074 · 1988-06-16

ApplicantKarlin Technology, Inc.
Decision Date1988-06-16
Product CodeGAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUCTION RETRACTORS is the device name listed in this FDA 510(k) record. The listed applicant is Karlin Technology, Inc.. It received FDA 510(k) clearance on 1988-06-16 under 510(k) number K882074. The device is classified under product code GAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUCTION RETRACTORS?

SUCTION RETRACTORS is a medical device that received FDA 510(k) clearance on 1988-06-16. The listed applicant is Karlin Technology, Inc.. The 510(k) number is K882074.

When did SUCTION RETRACTORS receive FDA 510(k) clearance?

SUCTION RETRACTORS received FDA 510(k) clearance on 1988-06-16, under 510(k) number K882074.

Who is the listed applicant for SUCTION RETRACTORS?

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

What is the FDA product code for SUCTION RETRACTORS?

The FDA product code for SUCTION RETRACTORS is GAD.

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Other records listing Karlin Technology, 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.

K903969SUCTION RETRACTOR(TOWER ATTACH.)FOR CRANK FRAM RETK893203BONE SCREWK893201BONE PLATEK882525SPINAL MICROKNIFEK882519X-RAY MARKERK882073SPINAL NEEDLE

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Related Devices (Code: GAD)

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.

K152538JRP Wound SpreaderJ.R. Parker, LLCK151104OTELO LLSpineartK132645THORATRAK MICS RETRACTOR SYSTEM, RACK, BLADESMedtronic, Inc.K071775DASHEzsurgicalK050256APPLE MEDICAL/OB MOBIUS ELASTIC RETRACTORApple Medical Corp.K043602QUADRANT RETRACTOR SYSTEMMedtronic Sofamor Danek

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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