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FDA 510(k)

PROCEDURAL STRECHER WITH INTELLIDRIVE P8000

K-Number: K112502 · 2011-09-19

ApplicantHill-Rom Co.
Decision Date2011-09-19
Product CodeINK
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PROCEDURAL STRECHER WITH INTELLIDRIVE P8000 is the device name listed in this FDA 510(k) record. The listed applicant is Hill-Rom Co.. It received FDA 510(k) clearance on 2011-09-19 under 510(k) number K112502. The device is classified under product code INK. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROCEDURAL STRECHER WITH INTELLIDRIVE P8000?

PROCEDURAL STRECHER WITH INTELLIDRIVE P8000 is a medical device that received FDA 510(k) clearance on 2011-09-19. The listed applicant is Hill-Rom Co.. The 510(k) number is K112502.

When did PROCEDURAL STRECHER WITH INTELLIDRIVE P8000 receive FDA 510(k) clearance?

PROCEDURAL STRECHER WITH INTELLIDRIVE P8000 received FDA 510(k) clearance on 2011-09-19, under 510(k) number K112502.

Who is the listed applicant for PROCEDURAL STRECHER WITH INTELLIDRIVE P8000?

The FDA 510(k) record lists Hill-Rom Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROCEDURAL STRECHER WITH INTELLIDRIVE P8000?

The FDA product code for PROCEDURAL STRECHER WITH INTELLIDRIVE P8000 is INK.

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Related Devices (Code: INK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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