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FDA 510(k)

ENDOSCOPY TABLE 1532 ENDOSTAR

K-Number: K873272 · 1987-09-08

ApplicantStierlen-Maquet AG
Decision Date1987-09-08
Product CodeBWN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPY TABLE 1532 ENDOSTAR is the device name listed in this FDA 510(k) record. The listed applicant is Stierlen-Maquet AG. It received FDA 510(k) clearance on 1987-09-08 under 510(k) number K873272. The device is classified under product code BWN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSCOPY TABLE 1532 ENDOSTAR?

ENDOSCOPY TABLE 1532 ENDOSTAR is a medical device that received FDA 510(k) clearance on 1987-09-08. The listed applicant is Stierlen-Maquet AG. The 510(k) number is K873272.

When did ENDOSCOPY TABLE 1532 ENDOSTAR receive FDA 510(k) clearance?

ENDOSCOPY TABLE 1532 ENDOSTAR received FDA 510(k) clearance on 1987-09-08, under 510(k) number K873272.

Who is the listed applicant for ENDOSCOPY TABLE 1532 ENDOSTAR?

The FDA 510(k) record lists Stierlen-Maquet AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOSCOPY TABLE 1532 ENDOSTAR?

The FDA product code for ENDOSCOPY TABLE 1532 ENDOSTAR is BWN.

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Other records listing Stierlen-Maquet AG as applicant

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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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