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FDA 510(k)

STAMEY NEEDLE

K-Number: K884553 · 1988-11-14

ApplicantCook Ob/Gyn
Decision Date1988-11-14
Product CodeGEJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STAMEY NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Cook Ob/Gyn. It received FDA 510(k) clearance on 1988-11-14 under 510(k) number K884553. The device is classified under product code GEJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAMEY NEEDLE?

STAMEY NEEDLE is a medical device that received FDA 510(k) clearance on 1988-11-14. The listed applicant is Cook Ob/Gyn. The 510(k) number is K884553.

When did STAMEY NEEDLE receive FDA 510(k) clearance?

STAMEY NEEDLE received FDA 510(k) clearance on 1988-11-14, under 510(k) number K884553.

Who is the listed applicant for STAMEY NEEDLE?

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

What is the FDA product code for STAMEY NEEDLE?

The FDA product code for STAMEY NEEDLE is GEJ.

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Other records listing Cook Ob/Gyn as applicant

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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Related Devices (Code: GEJ)

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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