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FDA 510(k)

RECTAL TUBE DEVICE

K-Number: K760886 · 1976-12-09

ApplicantVan Sickle Plastics Co.
Decision Date1976-12-09
Product CodeEXB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

RECTAL TUBE DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Van Sickle Plastics Co.. It received FDA 510(k) clearance on 1976-12-09 under 510(k) number K760886. The device is classified under product code EXB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RECTAL TUBE DEVICE?

RECTAL TUBE DEVICE is a medical device that received FDA 510(k) clearance on 1976-12-09. The listed applicant is Van Sickle Plastics Co.. The 510(k) number is K760886.

When did RECTAL TUBE DEVICE receive FDA 510(k) clearance?

RECTAL TUBE DEVICE received FDA 510(k) clearance on 1976-12-09, under 510(k) number K760886.

Who is the listed applicant for RECTAL TUBE DEVICE?

The FDA 510(k) record lists Van Sickle Plastics Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RECTAL TUBE DEVICE?

The FDA product code for RECTAL TUBE DEVICE is EXB.

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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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