LAPOROTOMY SPONGE— 510(k) K780806

Name: FDA 510(k) clearance K780806
Creator: U.S. Food and Drug Administration
Published: 1978-06-22

Substantially Equivalent

Abco Dealers, Inc.

FDA 510(k) clearance K780806 for LAPOROTOMY SPONGE, Substantially Equivalent on 1978-06-22. Applicant: Abco Dealers, Inc.. Device class: Unclassified.

Clearance details

Applicant: Abco Dealers, Inc.
Product code: Code EFQ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1978-05-10
Decision date: 1978-06-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EFQ

view all

K991757 — NON-ABSORBABLE GAUZE FOR EXTERNAL USE, STERILE AND NON STERILE1999-08-12
K991215 — SYMTEX GAUZE PADS (1'S) AND SYMTEX GAUZE SPONGES STERILE 2'S AND STERILE 10'S1999-06-11
K990974 — VITOP DRESSING1999-06-09
K990584 — GAUZE SPONGES: LAPAROTOMY SPONGE, X-RAY DETECTABLE1999-04-23
K984187 — CROSSTEX NON-WOVEN SPONGES1999-02-18

More clearances from Abco Dealers, Inc.

view all

K905025 — DIGITAL THERMOMETER KITS1991-02-07
K882304 — DIGITAL THERMOMETER SHEATHS (ORAL AND RECTAL)1988-07-12
K880892 — BLOOD COLLECTING NEEDLE AND HOLDERS1988-04-21
K880894 — ALLERGIST SYRINGES1988-03-31
K872875 — STRETCH GAUZE BANDAGES1987-09-04

Data sourced from openFDA. This site is unofficial and independent of the FDA.