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FDA 510(k)

DYNABITE LAPAROSCOPIC FORCEPS

K-Number: K944245 · 1994-11-15

ApplicantPortlyn Corp.
Decision Date1994-11-15
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DYNABITE LAPAROSCOPIC FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Portlyn Corp.. It received FDA 510(k) clearance on 1994-11-15 under 510(k) number K944245. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNABITE LAPAROSCOPIC FORCEPS?

DYNABITE LAPAROSCOPIC FORCEPS is a medical device that received FDA 510(k) clearance on 1994-11-15. The listed applicant is Portlyn Corp.. The 510(k) number is K944245.

When did DYNABITE LAPAROSCOPIC FORCEPS receive FDA 510(k) clearance?

DYNABITE LAPAROSCOPIC FORCEPS received FDA 510(k) clearance on 1994-11-15, under 510(k) number K944245.

Who is the listed applicant for DYNABITE LAPAROSCOPIC FORCEPS?

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

What is the FDA product code for DYNABITE LAPAROSCOPIC FORCEPS?

The FDA product code for DYNABITE LAPAROSCOPIC FORCEPS is HET.

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Other records listing Portlyn 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.

K970083DYNABITE HOT GI BIOPSY FORCEPSK951447DYNABITE CARDIOVASCULAR BIOPSY FORCEPSK952391DYNABITE UROLOGICAL FORCEPSK934506DYNABITE HYSTEROSCOPIC FORCEPSK901300BIOPSY FORCEPSK896147BIOPSY FORCEP (NON-ELECTRIC)

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Related Devices (Code: HET)

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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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