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FDA 510(k)

CERVICAL DILATORS PRATT,HAWKIN,KLEEGMAN,DENN.,VALL

K-Number: K891029 · 1989-03-17

ApplicantZinnanti Surgical Instruments, Inc.
Decision Date1989-03-17
Product CodeHDQ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CERVICAL DILATORS PRATT,HAWKIN,KLEEGMAN,DENN.,VALL is the device name listed in this FDA 510(k) record. The listed applicant is Zinnanti Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1989-03-17 under 510(k) number K891029. The device is classified under product code HDQ. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERVICAL DILATORS PRATT,HAWKIN,KLEEGMAN,DENN.,VALL?

CERVICAL DILATORS PRATT,HAWKIN,KLEEGMAN,DENN.,VALL is a medical device that received FDA 510(k) clearance on 1989-03-17. The listed applicant is Zinnanti Surgical Instruments, Inc.. The 510(k) number is K891029.

When did CERVICAL DILATORS PRATT,HAWKIN,KLEEGMAN,DENN.,VALL receive FDA 510(k) clearance?

CERVICAL DILATORS PRATT,HAWKIN,KLEEGMAN,DENN.,VALL received FDA 510(k) clearance on 1989-03-17, under 510(k) number K891029.

Who is the listed applicant for CERVICAL DILATORS PRATT,HAWKIN,KLEEGMAN,DENN.,VALL?

The FDA 510(k) record lists Zinnanti Surgical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CERVICAL DILATORS PRATT,HAWKIN,KLEEGMAN,DENN.,VALL?

The FDA product code for CERVICAL DILATORS PRATT,HAWKIN,KLEEGMAN,DENN.,VALL is HDQ.

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Other records listing Zinnanti Surgical Instruments, Inc. as applicant

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Related Devices (Code: HDQ)

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.

K930034CERVICAL DILATORS:PRATT,HAWKIN,KLEEGMAN,DENNISTONThomasville Medical Assoc.K896701TEFLON CERVICAL ACCESS SETCook Ob/GynK890377FIXED-SIZE UTERINE DILATORKinetic Medical ProductsK811568CERVICAL DILATORGynemetrics, Inc.K791277MODEL 6500 EXTRACTION IRRIGATION SYSCavitron Corp.

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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