INFLATABLE AIR SPLINTS— 510(k) K853600

Substantially Equivalent

Hospitak, Inc.

FDA 510(k) clearance K853600 for INFLATABLE AIR SPLINTS, Substantially Equivalent on 1985-09-19. Applicant: Hospitak, Inc.. Device class: 1.

Clearance details

Applicant: Hospitak, Inc.
Product code: Code FZF
Device class: Class 1
Regulation: 21 CFR 878.3900
Advisory panel: General, Plastic Surgery
Date received: 1985-08-27
Decision date: 1985-09-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lindenhurst, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FZF

K881516 — COMPRESAID1988-04-29
K874050 — INFLATABLE FOOT & ANKLE SPLINT1987-11-23
K874051 — INFLATABLE FULL LEG SPLINT1987-11-23
K874052 — INFLATABLE HALF LEG SPLINT1987-11-23
K874053 — INFLATABLE FULL ARM SPLINT1987-11-23

More clearances from Hospitak, Inc.

K955483 — TRACH MASK MODEL (245, 246)1996-02-28
K954787 — ILLUMINATOR1996-01-31
K953619 — WARM N WET HME W/LUER ADAPTER1995-08-25
K953620 — WARM N WET HMEF W/LUER ADAPTER1995-08-25
K915750 — DISPOSABLE BACTERIAL BREATHNG FILTER1994-11-30

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