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Pilling IPN008491

by Teleflex Incorporated 2 variants

Pilling IPN008491 (522581) is a Class II device made by Teleflex Incorporated, cleared under FDA 510(k) K861921 on 2 Jun 1986 and listed in FDA GUDID since 4 Sep 2020 (UDI-DI 24026704715446), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K861921

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number24026704715446 UDI-DI Date4 Sep 2020ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK861921 Date2 Jun 1986DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K861921 decided 2 Jun 1986 Active
  • FDA GUDID UDI-DI 24026704715446 listed 4 Sep 2020 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K861921
  2. Listed FDA GUDID 24026704715446

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Pilling
Generic name
Rigid optical bronchoscope
Model / Ref / Catalog
IPN008491, 522581
Primary DI / UDI-DI
24026704715446
510(k) Number
FDA product code
LLO
GMDN term
Rigid optical bronchoscope
Device class
Class II
Regulation number
874.4500
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 400 Millimeter

Related devices

Category: Rigid optical bronchoscope

Cleared under the same submission (K861921)

and 8 more cleared under K861921

Similar devices

Other devices filed under FDA product code LLO (LASER, NEODYMIUM:YAG, PULMONARY SURGERY).

Other devices from Teleflex Incorporated

  • Arrow IPNB00820 Open recall

    Class II

  • Arrow IPNB00826 Open recall

    Class II

  • Arrow IPNB00822 Open recall

    Class II

  • Arrow IPNB00827 Open recall

    Class II

See all devices from Teleflex Incorporated →

Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)