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FDA 510(k)

ANSPACH LUBRICATING SYSTEM II

K-Number: K970530 · 1997-05-05

ApplicantThe Anspach Effort, Inc.
Decision Date1997-05-05
Product CodeGEY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ANSPACH LUBRICATING SYSTEM II 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 1997-05-05 under 510(k) number K970530. 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 ANSPACH LUBRICATING SYSTEM II?

ANSPACH LUBRICATING SYSTEM II is a medical device that received FDA 510(k) clearance on 1997-05-05. The listed applicant is The Anspach Effort, Inc.. The 510(k) number is K970530.

When did ANSPACH LUBRICATING SYSTEM II receive FDA 510(k) clearance?

ANSPACH LUBRICATING SYSTEM II received FDA 510(k) clearance on 1997-05-05, under 510(k) number K970530.

Who is the listed applicant for ANSPACH LUBRICATING SYSTEM II?

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 ANSPACH LUBRICATING SYSTEM II?

The FDA product code for ANSPACH LUBRICATING SYSTEM II 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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