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FDA 510(k)

THERMO-PLASTIC SHAVER BLADES

K-Number: K963332 · 1996-10-11

ApplicantStryker Endoscopy
Decision Date1996-10-11
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

THERMO-PLASTIC SHAVER BLADES is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Endoscopy. It received FDA 510(k) clearance on 1996-10-11 under 510(k) number K963332. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THERMO-PLASTIC SHAVER BLADES?

THERMO-PLASTIC SHAVER BLADES is a medical device that received FDA 510(k) clearance on 1996-10-11. The listed applicant is Stryker Endoscopy. The 510(k) number is K963332.

When did THERMO-PLASTIC SHAVER BLADES receive FDA 510(k) clearance?

THERMO-PLASTIC SHAVER BLADES received FDA 510(k) clearance on 1996-10-11, under 510(k) number K963332.

Who is the listed applicant for THERMO-PLASTIC SHAVER BLADES?

The FDA 510(k) record lists Stryker Endoscopy as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THERMO-PLASTIC SHAVER BLADES?

The FDA product code for THERMO-PLASTIC SHAVER BLADES is HRX.

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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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