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FDA 510(k)

SULKY SPECIAL

K-Number: K863450 · 1986-10-23

ApplicantAsc Corp.
Decision Date1986-10-23
Product CodeLBE
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SULKY SPECIAL is the device name listed in this FDA 510(k) record. The listed applicant is Asc Corp.. It received FDA 510(k) clearance on 1986-10-23 under 510(k) number K863450. The device is classified under product code LBE. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SULKY SPECIAL?

SULKY SPECIAL is a medical device that received FDA 510(k) clearance on 1986-10-23. The listed applicant is Asc Corp.. The 510(k) number is K863450.

When did SULKY SPECIAL receive FDA 510(k) clearance?

SULKY SPECIAL received FDA 510(k) clearance on 1986-10-23, under 510(k) number K863450.

Who is the listed applicant for SULKY SPECIAL?

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

What is the FDA product code for SULKY SPECIAL?

The FDA product code for SULKY SPECIAL is LBE.

Related Clinical Trials

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Related Devices (Code: LBE)

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.

K223533Little Wave Arc; Little Wave FlipKi Mobility, LLCK130644PEDIATRIC FOLDING WHEELCHAIRColumbia Medical Mfg, LLCK862888PERAMBULATOR (STROLLER)Mednet, Inc.K840250CARRIERConvaid Products, Inc.K820591MECHANICAL CHAIRKaye Products, Inc.K810676CONVAID CRUISER CP4MConvaid Products, 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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