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FDA 510(k)

AUTO LUBE SYSTEM

K-Number: K940535 · 1994-03-21

ApplicantThe Anspach Effort, Inc.
Decision Date1994-03-21
Product CodeGEY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

AUTO LUBE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is The Anspach Effort, Inc.. It received FDA 510(k) clearance on 1994-03-21 under 510(k) number K940535. The device is classified under product code GEY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTO LUBE SYSTEM?

AUTO LUBE SYSTEM is a medical device that received FDA 510(k) clearance on 1994-03-21. The listed applicant is The Anspach Effort, Inc.. The 510(k) number is K940535.

When did AUTO LUBE SYSTEM receive FDA 510(k) clearance?

AUTO LUBE SYSTEM received FDA 510(k) clearance on 1994-03-21, under 510(k) number K940535.

Who is the listed applicant for AUTO LUBE SYSTEM?

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

What is the FDA product code for AUTO LUBE SYSTEM?

The FDA product code for AUTO LUBE SYSTEM is GEY.

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Other records listing The Anspach Effort, 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.

K220485Wireless Hand Control, EG1A (WIRELESS-HC), Receiver for Wireless Hand Control, EG1A (RECEIVER-HC)K183545Anspach Helix Dissection ToolsK180063OCM-G1 AttachmentK131053ANSPACH XMAX, EMAX2 AND EMAX2 PLUS SYSTEM WITH OTOLOGIC ATTACHMENT SYSTEMK113476ANSPACH DISSECTION TOOLSK082637CRANIAL PERFORATOR

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Related Devices (Code: GEY)

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.

K050519ADVANCED TURBO DRIVE SYSTEMLinvatec Corp.K020621ARTHROCARE CONTROLLER; ARTHROCARE CABLE; FOOT CONTROL; POWER CORD; WANDSArthrocare Corp.K012738SYMPHONY GRAFT DELIVERY SYSTEM (GDS)DepuyacromedK972308MEDNEXT 1000 DRILLMednext, Inc.K971941AQUA SPRAYBoyd Industries, Inc.K971782BONE AND MARROW COLLECTION SYSTEM KITBiomedical Ent., 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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