Bahama Blade 0600-1001-000

No FDA recalls on record, checked 23 Oct 2026.

Trade Name

Bahama Blade

Generic Name

Scalpel, single-use

Model / Ref / Catalog

0600-1001-000

Primary DI / UDI-DI

00817984010303

FDA Product Code

LXH

GMDN Term

Scalpel, single-use

Device Class

Class I

Regulation Number

888.4540

GUDID distribution status

Not in Commercial Distribution

• Tubalgator

  Class II

  FDA 510(k) K113080 Active Cleared 29 Jun 2012

• Insufflation Tubing

  Class II

  FDA 510(k) K925691 Active Cleared 23 Sep 1993

• Graspers

  Class II

  FDA 510(k) K935382 Active Cleared 15 Feb 1994

• Insufflator, Laparoscopic

  Class II

  FDA 510(k) K920959 Active Cleared 13 Jul 1992

• Electro-Lube

  Class II

  FDA 510(k) K033880 Active Cleared 10 Mar 2004

• Mectra Trocar

  Class II

  FDA 510(k) K934547 Active Cleared 18 Feb 1994

See all devices from Mectra Labs, Inc. →