Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

3M(TM) SURGICAL SLIPPER, 9660 SERIES

K-Number: K946162 · 1995-01-24

ApplicantWahl Clipper Corp.
Decision Date1995-01-24
Product CodeLWK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

3M(TM) SURGICAL SLIPPER, 9660 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Wahl Clipper Corp.. It received FDA 510(k) clearance on 1995-01-24 under 510(k) number K946162. The device is classified under product code LWK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3M(TM) SURGICAL SLIPPER, 9660 SERIES?

3M(TM) SURGICAL SLIPPER, 9660 SERIES is a medical device that received FDA 510(k) clearance on 1995-01-24. The listed applicant is Wahl Clipper Corp.. The 510(k) number is K946162.

When did 3M(TM) SURGICAL SLIPPER, 9660 SERIES receive FDA 510(k) clearance?

3M(TM) SURGICAL SLIPPER, 9660 SERIES received FDA 510(k) clearance on 1995-01-24, under 510(k) number K946162.

Who is the listed applicant for 3M(TM) SURGICAL SLIPPER, 9660 SERIES?

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

What is the FDA product code for 3M(TM) SURGICAL SLIPPER, 9660 SERIES?

The FDA product code for 3M(TM) SURGICAL SLIPPER, 9660 SERIES is LWK.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Wahl Clipper Corp. 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.

K944909WAHL FRESH FACEK950701WAHL SPORTS RELIEF HOT/COLD MASSAGER ROLLERK944024STIMU-TAPK941412WAHL COMPACT COMFORT MASSAGERK940683WAHL(R) ULTRA COMFORT MASSAGER SPEC #89ISAK940837WAHL(R) FOOT COMFORT MASSAGER

View all 8 devices →

Related Devices (Code: LWK)

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.

K910524SURGICAL CLIPPERBaxter Healthcare CorpK874370SURGICAL PREP RAZORDerma-Safe Co.K874234SURGICAL PREP RAZOR, STRAIGHT TYPEDerma-Safe Co.

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.

↑