Cap, Clarion Nurses, Style Bouffant 21

FDA 510(k) K770258 · Sherwood Medical Industries

Substantially Equivalent

510(k) numberK770258

Submission

Device name
Cap, Clarion Nurses, Style Bouffant 21
Applicant
Sherwood Medical Industries
Mchenry, IL, US
Received
February 11, 1977
Decision date
March 7, 1977
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FYF – Cap, Surgical
Device class
Class I (low risk)
Regulation
21 CFR 878.4040
Specialty
General, Plastic Surgery

Other 510(k)s with product code FYF

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K954556Surgical CapFYF · Traditional Thai Disposable Products Co., Ltd.03/12/1996SE
K954455Niomed Bouffant CapsFYF · Traditional Amerasia Corp.01/23/1996SE
K954454Niomed Surgical HoodFYF · Traditional Amerasia Corp.01/23/1996SE
K953879Surgeon's CapFYF · Traditional American Threshold Industries, Inc.01/05/1996SE
K953878Bouffant CapFYF · Traditional American Threshold Industries, Inc.01/05/1996SE
K913700Disposable Bouffant CapFYF · Traditional Gem Nonwovews, Inc.10/04/1991SE
K882346Instrument Protect-A-Caps, Aka: Tip/Instru. GuardFYF · Traditional Nordbye, Milchman, Barlage06/30/1988SE
K882284Surgeons CapFYF · Traditional A Plus International, Inc.06/23/1988SE

More from A Plus International, Inc.

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K801071Lancer Glucose Rate Reagent KitCGA · Traditional 05/23/1980SE
K792014Lancer L-Ina Buffer, Polymer, Wash SoluJZW · Traditional 11/13/1979SE
K792013Lancer L-Ina Human Reference SerumJIX · Traditional 11/13/1979SE
K782077Lancer Ice CubeJRM · Traditional 04/03/1979SE
K790523Argyle Esophageal StethoscopeBZW · Traditional 03/27/1979SE
K790196Monoject Arterial Blood Sampling DeviceCBT · Traditional 03/13/1979SE
K790197Reagent Kit, Lancer GlucoseJJF · Traditional 03/12/1979SE
K781459Monoject Scale MagnifierHJY · Traditional 10/24/1978SE
K781060Monoject Endosseous Dental ImplantDZE · Traditional 08/14/1978SE

Questions and answers

When was Cap, Clarion Nurses, Style Bouffant 21 cleared by the FDA?

Cap, Clarion Nurses, Style Bouffant 21 (K770258) received a 510(k) decision of Substantially Equivalent on March 7, 1977, 24 days after the submission was received.

What is the product code of K770258?

The FDA product code is FYF – Cap, Surgical, a Class I (low risk) device regulated under 21 CFR 878.4040.