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Hvo Hvo-5002

by H V O GUDID

Listed (no authorization) FDA GUDID database listing only

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860007847806 UDI-DIDate20 Apr 2026ListedStatusIn distribution

Coverage

1 jurisdiction

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  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
Hvo
Generic Name
Patient surgical drape, single-use
Model / Ref / Catalog
HVO-5002
Primary DI / UDI-DI
00860007847806
510(k) Number
FDA Product Code
KKX
GMDN Term
Patient surgical drape, single-use
Device Class
Class II
Regulation Number
878.4370
Commercial Distribution
In Commercial Distribution
Sterilization Method
Ethylene Oxide

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No