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FDA 510(k)

SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPS

K-Number: K930773 · 1994-07-28

ApplicantSymbiosis Corp.
Decision Date1994-07-28
Product CodeHFB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Symbiosis Corp.. It received FDA 510(k) clearance on 1994-07-28 under 510(k) number K930773. The device is classified under product code HFB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPS?

SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPS is a medical device that received FDA 510(k) clearance on 1994-07-28. The listed applicant is Symbiosis Corp.. The 510(k) number is K930773.

When did SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPS receive FDA 510(k) clearance?

SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPS received FDA 510(k) clearance on 1994-07-28, under 510(k) number K930773.

Who is the listed applicant for SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPS?

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

What is the FDA product code for SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPS?

The FDA product code for SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPS is HFB.

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Other records listing Symbiosis Corp. 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.

K955119SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODESK953453SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODESK953242SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODESK952432SYMBIOSIS BIPOLAR FORCEPSK951387SYMBIOSIS BIPOLAR SCISSORSK950286SYMBIOSIS BIPOLAR SCISSORS

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Related Devices (Code: HFB)

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.

K011488SPIRABRUSH CX BIOPSY INSTRUMENTTrylon Corp.K944444CIT BIOPSY PUNCHESChirurgische InstrumenteK933767FORCEPS, BIOPSY GYNECOLOGICAL INSTRU/BIOPSYMahe-MedizintechnikK926595OWENS BIOPSY FORCEPSOwens Industries, Inc.K926527ROTO FIT BIOPSY FORCEPSThomasville Medical Assoc.K930036THOMAS MEDICAL BIOPSY FORCEPSThomasville Medical Assoc.

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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