Rocket Sex Crime Kit

FDA 510(k) K883805 · A & A Medical, Inc.

Substantially Equivalent

510(k) numberK883805

Submission

Device name
Rocket Sex Crime Kit
Applicant
A & A Medical, Inc.
Branford, CT, US
Received
September 7, 1988
Decision date
January 31, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FMC – Patient Examination Glove
Device class
Class I (low risk)
Regulation
21 CFR 880.6250
Specialty
General Hospital

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Questions and answers

When was Rocket Sex Crime Kit cleared by the FDA?

Rocket Sex Crime Kit (K883805) received a 510(k) decision of Substantially Equivalent on January 31, 1989, 146 days after the submission was received.

What is the product code of K883805?

The FDA product code is FMC – Patient Examination Glove, a Class I (low risk) device regulated under 21 CFR 880.6250.