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FDA 510(k)

OBSTI-HOOK

K-Number: K951148 · 1995-06-09

ApplicantOnli
Decision Date1995-06-09
Product CodeHGE
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

OBSTI-HOOK is the device name listed in this FDA 510(k) record. The listed applicant is Onli. It received FDA 510(k) clearance on 1995-06-09 under 510(k) number K951148. The device is classified under product code HGE. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OBSTI-HOOK?

OBSTI-HOOK is a medical device that received FDA 510(k) clearance on 1995-06-09. The listed applicant is Onli. The 510(k) number is K951148.

When did OBSTI-HOOK receive FDA 510(k) clearance?

OBSTI-HOOK received FDA 510(k) clearance on 1995-06-09, under 510(k) number K951148.

Who is the listed applicant for OBSTI-HOOK?

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

What is the FDA product code for OBSTI-HOOK?

The FDA product code for OBSTI-HOOK is HGE.

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Related Devices (Code: HGE)

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

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

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