FDA 510K Validation of Steam Sterilizer

Project Description

URGENT
Medical Device Company needs FDA GMP Contract Laboratory and Consultant for validation with an Overkill Method for wet heat high pressure autoclave (steam sterilizer). We need it for FDA 510K submission.
We have the validation of sterilization according to ISO 17665-1.
We are in a crunch, and we would not mind to pay for expedited completion of the request.
What possible dates you could accommodate and what would be the pricing?